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esv2764031

  • Variant Calls:36
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,337,937

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 9248 SVs from 125 studies. See in: genome view    
Remapped(Score: Pass):61,081,249-63,419,185Question Mark
Overlapping variant regions from other studies: 8893 SVs from 122 studies. See in: genome view    
Remapped(Score: Pass):61,063,974-62,879,563Question Mark
Overlapping variant regions from other studies: 2788 SVs from 34 studies. See in: genome view    
Submitted genomic61,067,916-62,516,998Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartOuter Stop
esv2764031RemappedPassGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr761,081,24963,419,185
esv2764031RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr761,063,97462,879,563
esv2764031Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000007.12Chr761,067,91662,516,998

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv6990822copy number gainSW_1436SNP arraySNP genotyping analysis64
essv6990824copy number gainSW_1482SNP arraySNP genotyping analysis31
essv6990828copy number gainSW_0200SNP arraySNP genotyping analysis51
essv6990829copy number lossSW_0818SNP arraySNP genotyping analysis30
essv6990830copy number gainSW_1404SNP arraySNP genotyping analysis44
essv6990825copy number lossSW_0116SNP arraySNP genotyping analysis34
essv6990826copy number lossSW_1095SNP arraySNP genotyping analysis40
essv6990831copy number gainSW_1481SNP arraySNP genotyping analysis19
essv6990832copy number lossSW_1088SNP arraySNP genotyping analysis37
essv6990833copy number gainSW_0103SNP arraySNP genotyping analysis37
essv6990835copy number gainSW_0618SNP arraySNP genotyping analysis23
essv6990836copy number gainSW_1045SNP arraySNP genotyping analysis49
essv6990837copy number gainSW_1116SNP arraySNP genotyping analysis50
essv6990838copy number gainSW_0225SNP arraySNP genotyping analysis18
essv6990839copy number gainSW_0717SNP arraySNP genotyping analysis24
essv6990840copy number gainSW_1152SNP arraySNP genotyping analysis19
essv6990841copy number gainSW_1287SNP arraySNP genotyping analysis27
essv6990842copy number gainSW_0815SNP arraySNP genotyping analysis46
essv6990843copy number lossSW_0059SNP arraySNP genotyping analysis36
essv6990844copy number lossSW_0606SNP arraySNP genotyping analysis46
essv6990846copy number lossSW_0677SNP arraySNP genotyping analysis32
essv6990847copy number lossSW_0831SNP arraySNP genotyping analysis42
essv6990848copy number lossSW_0855SNP arraySNP genotyping analysis29
essv6990849copy number lossSW_1127SNP arraySNP genotyping analysis34
essv6990850copy number lossSW_1131SNP arraySNP genotyping analysis31
essv6990851copy number lossSW_1168SNP arraySNP genotyping analysis32
essv6990852copy number lossSW_1212SNP arraySNP genotyping analysis29
essv6990853copy number gainSW_1480SNP arraySNP genotyping analysis37
essv6990854copy number lossSW_0791SNP arraySNP genotyping analysis38
essv6990855copy number lossSW_1065SNP arraySNP genotyping analysis28
essv6990858copy number gainSW_1455SNP arraySNP genotyping analysis39
essv6990859copy number gainSW_0076SNP arraySNP genotyping analysis46
essv6990860copy number lossSW_0185SNP arraySNP genotyping analysis43
essv6990861copy number gainSW_0147SNP arraySNP genotyping analysis33
essv6990862copy number lossSW_0172SNP arraySNP genotyping analysis45
essv6990827copy number lossSW_0255SNP arraySNP genotyping analysis31

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
essv6990822RemappedPassNC_000007.14:g.(?_
61081249)_(6235886
4_?)dup
GRCh38.p12First PassNC_000007.14Chr761,081,24962,358,864
essv6990824RemappedPassNC_000007.14:g.(?_
61081249)_(6286513
5_?)dup
GRCh38.p12First PassNC_000007.14Chr761,081,24962,865,135
essv6990828RemappedPassNC_000007.14:g.(?_
62209431)_(6229443
2_?)dup
GRCh38.p12First PassNC_000007.14Chr762,209,43162,294,432
essv6990829RemappedPassNC_000007.14:g.(?_
62209431)_(6229443
2_?)del
GRCh38.p12First PassNC_000007.14Chr762,209,43162,294,432
essv6990830RemappedPassNC_000007.14:g.(?_
62209431)_(6229443
2_?)dup
GRCh38.p12First PassNC_000007.14Chr762,209,43162,294,432
essv6990825RemappedPassNC_000007.14:g.(?_
62294433)_(6235886
4_?)del
GRCh38.p12First PassNC_000007.14Chr762,294,43362,358,864
essv6990826RemappedPassNC_000007.14:g.(?_
62294433)_(6235886
4_?)del
GRCh38.p12First PassNC_000007.14Chr762,294,43362,358,864
essv6990831RemappedGoodNC_000007.14:g.(?_
62294433)_(6327338
3_?)dup
GRCh38.p12First PassNC_000007.14Chr762,294,43363,273,383
essv6990832RemappedPassNC_000007.14:g.(?_
62316452)_(6235886
4_?)del
GRCh38.p12First PassNC_000007.14Chr762,316,45262,358,864
essv6990833RemappedPerfectNC_000007.14:g.(?_
62526795)_(6266369
6_?)dup
GRCh38.p12First PassNC_000007.14Chr762,526,79562,663,696
essv6990835RemappedPerfectNC_000007.14:g.(?_
62526795)_(6266369
6_?)dup
GRCh38.p12First PassNC_000007.14Chr762,526,79562,663,696
essv6990836RemappedPerfectNC_000007.14:g.(?_
62526795)_(6266369
6_?)dup
GRCh38.p12First PassNC_000007.14Chr762,526,79562,663,696
essv6990837RemappedPerfectNC_000007.14:g.(?_
62526795)_(6266369
6_?)dup
GRCh38.p12First PassNC_000007.14Chr762,526,79562,663,696
essv6990838RemappedPerfectNC_000007.14:g.(?_
62526795)_(6331022
9_?)dup
GRCh38.p12First PassNC_000007.14Chr762,526,79563,310,229
essv6990839RemappedPerfectNC_000007.14:g.(?_
62553947)_(6329232
3_?)dup
GRCh38.p12First PassNC_000007.14Chr762,553,94763,292,323
essv6990840RemappedPerfectNC_000007.14:g.(?_
62589052)_(6324603
8_?)dup
GRCh38.p12First PassNC_000007.14Chr762,589,05263,246,038
essv6990841RemappedPerfectNC_000007.14:g.(?_
62589052)_(6324603
8_?)dup
GRCh38.p12First PassNC_000007.14Chr762,589,05263,246,038
essv6990842RemappedPerfectNC_000007.14:g.(?_
62616923)_(6327338
3_?)dup
GRCh38.p12First PassNC_000007.14Chr762,616,92363,273,383
essv6990843RemappedPerfectNC_000007.14:g.(?_
62695960)_(6270189
6_?)del
GRCh38.p12First PassNC_000007.14Chr762,695,96062,701,896
essv6990844RemappedPerfectNC_000007.14:g.(?_
62695960)_(6270189
6_?)del
GRCh38.p12First PassNC_000007.14Chr762,695,96062,701,896
essv6990846RemappedPerfectNC_000007.14:g.(?_
62695960)_(6270189
6_?)del
GRCh38.p12First PassNC_000007.14Chr762,695,96062,701,896
essv6990847RemappedPerfectNC_000007.14:g.(?_
62695960)_(6270189
6_?)del
GRCh38.p12First PassNC_000007.14Chr762,695,96062,701,896
essv6990848RemappedPerfectNC_000007.14:g.(?_
62695960)_(6270189
6_?)del
GRCh38.p12First PassNC_000007.14Chr762,695,96062,701,896
essv6990849RemappedPerfectNC_000007.14:g.(?_
62695960)_(6270189
6_?)del
GRCh38.p12First PassNC_000007.14Chr762,695,96062,701,896
essv6990850RemappedPerfectNC_000007.14:g.(?_
62695960)_(6270189
6_?)del
GRCh38.p12First PassNC_000007.14Chr762,695,96062,701,896
essv6990851RemappedPerfectNC_000007.14:g.(?_
62695960)_(6270189
6_?)del
GRCh38.p12First PassNC_000007.14Chr762,695,96062,701,896
essv6990852RemappedPerfectNC_000007.14:g.(?_
62695960)_(6270189
6_?)del
GRCh38.p12First PassNC_000007.14Chr762,695,96062,701,896
essv6990853RemappedPerfectNC_000007.14:g.(?_
62695960)_(6270189
6_?)dup
GRCh38.p12First PassNC_000007.14Chr762,695,96062,701,896
essv6990854RemappedPerfectNC_000007.14:g.(?_
62695960)_(6272245
1_?)del
GRCh38.p12First PassNC_000007.14Chr762,695,96062,722,451
essv6990855RemappedPerfectNC_000007.14:g.(?_
62695960)_(6272245
1_?)del
GRCh38.p12First PassNC_000007.14Chr762,695,96062,722,451
essv6990858RemappedPerfectNC_000007.14:g.(?_
62835392)_(6283586
1_?)dup
GRCh38.p12First PassNC_000007.14Chr762,835,39262,835,861
essv6990859RemappedPerfectNC_000007.14:g.(?_
62835392)_(6293304
0_?)dup
GRCh38.p12First PassNC_000007.14Chr762,835,39262,933,040
essv6990860RemappedPerfectNC_000007.14:g.(?_
62904814)_(6290945
6_?)del
GRCh38.p12First PassNC_000007.14Chr762,904,81462,909,456
essv6990861RemappedPerfectNC_000007.14:g.(?_
63128783)_(6341918
5_?)dup
GRCh38.p12First PassNC_000007.14Chr763,128,78363,419,185
essv6990862RemappedPerfectNC_000007.14:g.(?_
63228970)_(6333242
3_?)del
GRCh38.p12First PassNC_000007.14Chr763,228,97063,332,423
essv6990827RemappedPassNT_187383.1:g.(?_3
31933)_(610898_?)d
el
GRCh38.p12Second PassNT_187383.1Chr16|NT_1
87383.1
331,933610,898
essv6990822RemappedPassNC_000007.13:g.(?_
61063974)_(6188812
8_?)dup
GRCh37.p13First PassNC_000007.13Chr761,063,97461,888,128
essv6990824RemappedPassNC_000007.13:g.(?_
61063974)_(6232551
3_?)dup
GRCh37.p13First PassNC_000007.13Chr761,063,97462,325,513
essv6990825RemappedPerfectNC_000007.13:g.(?_
61728407)_(6181578
0_?)del
GRCh37.p13First PassNC_000007.13Chr761,728,40761,815,780
essv6990826RemappedPerfectNC_000007.13:g.(?_
61728407)_(6182608
1_?)del
GRCh37.p13First PassNC_000007.13Chr761,728,40761,826,081
essv6990827RemappedPerfectNC_000007.13:g.(?_
61728407)_(6185837
5_?)del
GRCh37.p13First PassNC_000007.13Chr761,728,40761,858,375
essv6990828RemappedPerfectNC_000007.13:g.(?_
61728407)_(6188812
8_?)dup
GRCh37.p13First PassNC_000007.13Chr761,728,40761,888,128
essv6990829RemappedPerfectNC_000007.13:g.(?_
61728407)_(6188812
8_?)del
GRCh37.p13First PassNC_000007.13Chr761,728,40761,888,128
essv6990830RemappedPerfectNC_000007.13:g.(?_
61728407)_(6188812
8_?)dup
GRCh37.p13First PassNC_000007.13Chr761,728,40761,888,128
essv6990831RemappedPerfectNC_000007.13:g.(?_
61728407)_(6273376
1_?)dup
GRCh37.p13First PassNC_000007.13Chr761,728,40762,733,761
essv6990832RemappedPerfectNC_000007.13:g.(?_
61760703)_(6183205
7_?)del
GRCh37.p13First PassNC_000007.13Chr761,760,70361,832,057
essv6990833RemappedPerfectNC_000007.13:g.(?_
61987173)_(6212407
4_?)dup
GRCh37.p13First PassNC_000007.13Chr761,987,17362,124,074
essv6990835RemappedPerfectNC_000007.13:g.(?_
61987173)_(6212407
4_?)dup
GRCh37.p13First PassNC_000007.13Chr761,987,17362,124,074
essv6990836RemappedPerfectNC_000007.13:g.(?_
61987173)_(6212407
4_?)dup
GRCh37.p13First PassNC_000007.13Chr761,987,17362,124,074
essv6990837RemappedPerfectNC_000007.13:g.(?_
61987173)_(6212407
4_?)dup
GRCh37.p13First PassNC_000007.13Chr761,987,17362,124,074
essv6990838RemappedPerfectNC_000007.13:g.(?_
61987173)_(6277060
7_?)dup
GRCh37.p13First PassNC_000007.13Chr761,987,17362,770,607
essv6990839RemappedPerfectNC_000007.13:g.(?_
62014325)_(6275270
1_?)dup
GRCh37.p13First PassNC_000007.13Chr762,014,32562,752,701
essv6990840RemappedPerfectNC_000007.13:g.(?_
62049430)_(6270641
6_?)dup
GRCh37.p13First PassNC_000007.13Chr762,049,43062,706,416
essv6990841RemappedPerfectNC_000007.13:g.(?_
62049430)_(6270641
6_?)dup
GRCh37.p13First PassNC_000007.13Chr762,049,43062,706,416
essv6990842RemappedPerfectNC_000007.13:g.(?_
62077301)_(6273376
1_?)dup
GRCh37.p13First PassNC_000007.13Chr762,077,30162,733,761
essv6990843RemappedPerfectNC_000007.13:g.(?_
62156338)_(6216227
4_?)del
GRCh37.p13First PassNC_000007.13Chr762,156,33862,162,274
essv6990844RemappedPerfectNC_000007.13:g.(?_
62156338)_(6216227
4_?)del
GRCh37.p13First PassNC_000007.13Chr762,156,33862,162,274
essv6990846RemappedPerfectNC_000007.13:g.(?_
62156338)_(6216227
4_?)del
GRCh37.p13First PassNC_000007.13Chr762,156,33862,162,274
essv6990847RemappedPerfectNC_000007.13:g.(?_
62156338)_(6216227
4_?)del
GRCh37.p13First PassNC_000007.13Chr762,156,33862,162,274
essv6990848RemappedPerfectNC_000007.13:g.(?_
62156338)_(6216227
4_?)del
GRCh37.p13First PassNC_000007.13Chr762,156,33862,162,274
essv6990849RemappedPerfectNC_000007.13:g.(?_
62156338)_(6216227
4_?)del
GRCh37.p13First PassNC_000007.13Chr762,156,33862,162,274
essv6990850RemappedPerfectNC_000007.13:g.(?_
62156338)_(6216227
4_?)del
GRCh37.p13First PassNC_000007.13Chr762,156,33862,162,274
essv6990851RemappedPerfectNC_000007.13:g.(?_
62156338)_(6216227
4_?)del
GRCh37.p13First PassNC_000007.13Chr762,156,33862,162,274
essv6990852RemappedPerfectNC_000007.13:g.(?_
62156338)_(6216227
4_?)del
GRCh37.p13First PassNC_000007.13Chr762,156,33862,162,274
essv6990853RemappedPerfectNC_000007.13:g.(?_
62156338)_(6216227
4_?)dup
GRCh37.p13First PassNC_000007.13Chr762,156,33862,162,274
essv6990854RemappedPerfectNC_000007.13:g.(?_
62156338)_(6218282
9_?)del
GRCh37.p13First PassNC_000007.13Chr762,156,33862,182,829
essv6990855RemappedPerfectNC_000007.13:g.(?_
62156338)_(6218282
9_?)del
GRCh37.p13First PassNC_000007.13Chr762,156,33862,182,829
essv6990858RemappedPerfectNC_000007.13:g.(?_
62295770)_(6229623
9_?)dup
GRCh37.p13First PassNC_000007.13Chr762,295,77062,296,239
essv6990859RemappedPerfectNC_000007.13:g.(?_
62295770)_(6239341
8_?)dup
GRCh37.p13First PassNC_000007.13Chr762,295,77062,393,418
essv6990860RemappedPerfectNC_000007.13:g.(?_
62365192)_(6236983
4_?)del
GRCh37.p13First PassNC_000007.13Chr762,365,19262,369,834
essv6990861RemappedPerfectNC_000007.13:g.(?_
62589161)_(6287956
3_?)dup
GRCh37.p13First PassNC_000007.13Chr762,589,16162,879,563
essv6990862RemappedPerfectNC_000007.13:g.(?_
62689348)_(6279280
1_?)del
GRCh37.p13First PassNC_000007.13Chr762,689,34862,792,801
essv6990822Submitted genomicNC_000007.12:g.(?_
61067916)_(6152556
3_?)dup
NCBI36 (hg18)NC_000007.12Chr761,067,91661,525,563
essv6990824Submitted genomicNC_000007.12:g.(?_
61067916)_(6196294
8_?)dup
NCBI36 (hg18)NC_000007.12Chr761,067,91661,962,948
essv6990825Submitted genomicNC_000007.12:g.(?_
61365842)_(6145321
5_?)del
NCBI36 (hg18)NC_000007.12Chr761,365,84261,453,215
essv6990826Submitted genomicNC_000007.12:g.(?_
61365842)_(6146351
6_?)del
NCBI36 (hg18)NC_000007.12Chr761,365,84261,463,516
essv6990827Submitted genomicNC_000007.12:g.(?_
61365842)_(6149581
0_?)del
NCBI36 (hg18)NC_000007.12Chr761,365,84261,495,810
essv6990828Submitted genomicNC_000007.12:g.(?_
61365842)_(6152556
3_?)dup
NCBI36 (hg18)NC_000007.12Chr761,365,84261,525,563
essv6990829Submitted genomicNC_000007.12:g.(?_
61365842)_(6152556
3_?)del
NCBI36 (hg18)NC_000007.12Chr761,365,84261,525,563
essv6990830Submitted genomicNC_000007.12:g.(?_
61365842)_(6152556
3_?)dup
NCBI36 (hg18)NC_000007.12Chr761,365,84261,525,563
essv6990831Submitted genomicNC_000007.12:g.(?_
61365842)_(6237119
6_?)dup
NCBI36 (hg18)NC_000007.12Chr761,365,84262,371,196
essv6990832Submitted genomicNC_000007.12:g.(?_
61398138)_(6146949
2_?)del
NCBI36 (hg18)NC_000007.12Chr761,398,13861,469,492
essv6990833Submitted genomicNC_000007.12:g.(?_
61624608)_(6176150
9_?)dup
NCBI36 (hg18)NC_000007.12Chr761,624,60861,761,509
essv6990835Submitted genomicNC_000007.12:g.(?_
61624608)_(6176150
9_?)dup
NCBI36 (hg18)NC_000007.12Chr761,624,60861,761,509
essv6990836Submitted genomicNC_000007.12:g.(?_
61624608)_(6176150
9_?)dup
NCBI36 (hg18)NC_000007.12Chr761,624,60861,761,509
essv6990837Submitted genomicNC_000007.12:g.(?_
61624608)_(6176150
9_?)dup
NCBI36 (hg18)NC_000007.12Chr761,624,60861,761,509
essv6990838Submitted genomicNC_000007.12:g.(?_
61624608)_(6240804
2_?)dup
NCBI36 (hg18)NC_000007.12Chr761,624,60862,408,042
essv6990839Submitted genomicNC_000007.12:g.(?_
61651760)_(6239013
6_?)dup
NCBI36 (hg18)NC_000007.12Chr761,651,76062,390,136
essv6990840Submitted genomicNC_000007.12:g.(?_
61686865)_(6234385
1_?)dup
NCBI36 (hg18)NC_000007.12Chr761,686,86562,343,851
essv6990841Submitted genomicNC_000007.12:g.(?_
61686865)_(6234385
1_?)dup
NCBI36 (hg18)NC_000007.12Chr761,686,86562,343,851
essv6990842Submitted genomicNC_000007.12:g.(?_
61714736)_(6237119
6_?)dup
NCBI36 (hg18)NC_000007.12Chr761,714,73662,371,196
essv6990843Submitted genomicNC_000007.12:g.(?_
61793773)_(6179970
9_?)del
NCBI36 (hg18)NC_000007.12Chr761,793,77361,799,709
essv6990844Submitted genomicNC_000007.12:g.(?_
61793773)_(6179970
9_?)del
NCBI36 (hg18)NC_000007.12Chr761,793,77361,799,709
essv6990846Submitted genomicNC_000007.12:g.(?_
61793773)_(6179970
9_?)del
NCBI36 (hg18)NC_000007.12Chr761,793,77361,799,709
essv6990847Submitted genomicNC_000007.12:g.(?_
61793773)_(6179970
9_?)del
NCBI36 (hg18)NC_000007.12Chr761,793,77361,799,709
essv6990848Submitted genomicNC_000007.12:g.(?_
61793773)_(6179970
9_?)del
NCBI36 (hg18)NC_000007.12Chr761,793,77361,799,709
essv6990849Submitted genomicNC_000007.12:g.(?_
61793773)_(6179970
9_?)del
NCBI36 (hg18)NC_000007.12Chr761,793,77361,799,709
essv6990850Submitted genomicNC_000007.12:g.(?_
61793773)_(6179970
9_?)del
NCBI36 (hg18)NC_000007.12Chr761,793,77361,799,709
essv6990851Submitted genomicNC_000007.12:g.(?_
61793773)_(6179970
9_?)del
NCBI36 (hg18)NC_000007.12Chr761,793,77361,799,709
essv6990852Submitted genomicNC_000007.12:g.(?_
61793773)_(6179970
9_?)del
NCBI36 (hg18)NC_000007.12Chr761,793,77361,799,709
Showing 100 of 108

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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