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esv2761152

  • Variant Calls:30
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,307,774

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 9219 SVs from 125 studies. See in: genome view    
Remapped(Score: Pass):61,081,249-63,389,022Question Mark
Overlapping variant regions from other studies: 8864 SVs from 122 studies. See in: genome view    
Remapped(Score: Pass):61,063,974-62,849,400Question Mark
Overlapping variant regions from other studies: 2775 SVs from 34 studies. See in: genome view    
Submitted genomic61,067,916-62,486,835Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartOuter Stop
esv2761152RemappedPassGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr761,081,24963,389,022
esv2761152RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr761,063,97462,849,400
esv2761152Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000007.12Chr761,067,91662,486,835

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv7014712copy number gainRW_0574SNP arraySNP genotyping analysis32
essv7014713copy number lossRW_0012SNP arraySNP genotyping analysis41
essv7014714copy number gainRW_0036SNP arraySNP genotyping analysis46
essv7014715copy number gainRW_0504SNP arraySNP genotyping analysis34
essv7014716copy number lossRW_0263SNP arraySNP genotyping analysis54
essv7014717copy number lossRW_0061SNP arraySNP genotyping analysis54
essv7014739copy number lossRW_0546SNP arraySNP genotyping analysis50
essv7014738copy number lossRW_0655SNP arraySNP genotyping analysis45
essv7014736copy number lossRW_0111SNP arraySNP genotyping analysis65
essv7014734copy number lossRW_0117SNP arraySNP genotyping analysis52
essv7014731copy number lossRW_0115SNP arraySNP genotyping analysis50
essv7014728copy number lossRW_0196SNP arraySNP genotyping analysis67
essv7014729copy number lossRW_0522SNP arraySNP genotyping analysis37
essv7014720copy number lossRW_0138SNP arraySNP genotyping analysis34
essv7014721copy number lossRW_0648SNP arraySNP genotyping analysis52
essv7014723copy number lossRW_0002SNP arraySNP genotyping analysis76
essv7014724copy number lossRW_0107SNP arraySNP genotyping analysis48
essv7014725copy number lossRW_0568SNP arraySNP genotyping analysis36
essv7014726copy number lossRW_0609SNP arraySNP genotyping analysis25
essv7014735copy number lossRW_0217SNP arraySNP genotyping analysis62
essv7014732copy number lossRW_0358SNP arraySNP genotyping analysis42
essv7014727copy number lossRW_0179SNP arraySNP genotyping analysis63
essv7014718copy number lossRW_0018SNP arraySNP genotyping analysis54
essv7014719copy number lossRW_0509SNP arraySNP genotyping analysis17
essv7014730copy number gainRW_0597SNP arraySNP genotyping analysis26
essv7014740copy number gainRW_0509SNP arraySNP genotyping analysis17
essv7014741copy number gainRW_0650SNP arraySNP genotyping analysis25
essv7014742copy number gainRW_0506SNP arraySNP genotyping analysis43
essv7014743copy number gainRW_0603SNP arraySNP genotyping analysis49
essv7014737copy number lossRW_0323SNP arraySNP genotyping analysis42

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
essv7014712RemappedPassNC_000007.14:g.(?_
61081249)_(6235886
4_?)dup
GRCh38.p12First PassNC_000007.14Chr761,081,24962,358,864
essv7014713RemappedPassNC_000007.14:g.(?_
61578038)_(6237623
9_?)delNT_187383.1
:g.(?_331112)_(610
898_?)del
GRCh38.p12Second PassNC_000007.14Chr761,578,03862,376,239
essv7014714RemappedPassNT_187383.1:g.(?_3
31112)_(610898_?)d
upNC_000007.14:g.(
?_61578038)_(62376
239_?)dup
GRCh38.p12Second PassNC_000007.14Chr761,578,03862,376,239
essv7014715RemappedPassNT_187383.1:g.(?_3
31112)_(610898_?)d
upNC_000007.14:g.(
?_61578038)_(62376
239_?)dup
GRCh38.p12Second PassNC_000007.14Chr761,578,03862,376,239
essv7014716RemappedPassNC_000007.14:g.(?_
61578038)_(6237623
9_?)delNT_187383.1
:g.(?_331112)_(610
898_?)del
GRCh38.p12Second PassNC_000007.14Chr761,578,03862,376,239
essv7014717RemappedPassNC_000007.14:g.(?_
61578038)_(6237623
9_?)delNT_187383.1
:g.(?_331112)_(610
898_?)del
GRCh38.p12Second PassNC_000007.14Chr761,578,03862,376,239
essv7014739RemappedGoodNC_000007.14:g.(?_
62209431)_(6224727
0_?)del
GRCh38.p12First PassNC_000007.14Chr762,209,43162,247,270
essv7014738RemappedGoodNC_000007.14:g.(?_
62209431)_(6225125
7_?)del
GRCh38.p12First PassNC_000007.14Chr762,209,43162,251,257
essv7014736RemappedGoodNC_000007.14:g.(?_
62209431)_(6225805
7_?)del
GRCh38.p12First PassNC_000007.14Chr762,209,43162,258,057
essv7014734RemappedGoodNC_000007.14:g.(?_
62209431)_(6226110
4_?)del
GRCh38.p12First PassNC_000007.14Chr762,209,43162,261,104
essv7014731RemappedGoodNC_000007.14:g.(?_
62209431)_(6228538
9_?)del
GRCh38.p12First PassNC_000007.14Chr762,209,43162,285,389
essv7014728RemappedGoodNC_000007.14:g.(?_
62209431)_(6228995
9_?)del
GRCh38.p12First PassNC_000007.14Chr762,209,43162,289,959
essv7014729RemappedGoodNC_000007.14:g.(?_
62209431)_(6228995
9_?)del
GRCh38.p12First PassNC_000007.14Chr762,209,43162,289,959
essv7014720RemappedPassNC_000007.14:g.(?_
62209431)_(6229443
2_?)del
GRCh38.p12First PassNC_000007.14Chr762,209,43162,294,432
essv7014721RemappedPassNC_000007.14:g.(?_
62209431)_(6229443
2_?)del
GRCh38.p12First PassNC_000007.14Chr762,209,43162,294,432
essv7014723RemappedPassNC_000007.14:g.(?_
62209431)_(6229443
2_?)del
GRCh38.p12First PassNC_000007.14Chr762,209,43162,294,432
essv7014724RemappedPassNC_000007.14:g.(?_
62209431)_(6229443
2_?)del
GRCh38.p12First PassNC_000007.14Chr762,209,43162,294,432
essv7014725RemappedPassNC_000007.14:g.(?_
62209431)_(6229443
2_?)del
GRCh38.p12First PassNC_000007.14Chr762,209,43162,294,432
essv7014726RemappedPassNC_000007.14:g.(?_
62209431)_(6229443
2_?)del
GRCh38.p12First PassNC_000007.14Chr762,209,43162,294,432
essv7014735RemappedGoodNC_000007.14:g.(?_
62239187)_(6225805
7_?)del
GRCh38.p12First PassNC_000007.14Chr762,239,18762,258,057
essv7014732RemappedGoodNC_000007.14:g.(?_
62239187)_(6227146
7_?)del
GRCh38.p12First PassNC_000007.14Chr762,239,18762,271,467
essv7014727RemappedGoodNC_000007.14:g.(?_
62246376)_(6228995
9_?)del
GRCh38.p12First PassNC_000007.14Chr762,246,37662,289,959
essv7014718RemappedPassNC_000007.14:g.(?_
62294433)_(6235886
4_?)del
GRCh38.p12First PassNC_000007.14Chr762,294,43362,358,864
essv7014719RemappedPassNC_000007.14:g.(?_
62294433)_(6235886
4_?)del
GRCh38.p12First PassNC_000007.14Chr762,294,43362,358,864
essv7014730RemappedPassNC_000007.14:g.(?_
62506780)_(6297890
3_?)dup
GRCh38.p12First PassNC_000007.14Chr762,506,78062,978,903
essv7014740RemappedPassNC_000007.14:g.(?_
62506780)_(6333242
3_?)dup
GRCh38.p12First PassNC_000007.14Chr762,506,78063,332,423
essv7014741RemappedPerfectNC_000007.14:g.(?_
62526795)_(6279210
3_?)dup
GRCh38.p12First PassNC_000007.14Chr762,526,79562,792,103
essv7014742RemappedPerfectNC_000007.14:g.(?_
62655626)_(6270189
6_?)dup
GRCh38.p12First PassNC_000007.14Chr762,655,62662,701,896
essv7014743RemappedPerfectNC_000007.14:g.(?_
63202573)_(6338902
2_?)dup
GRCh38.p12First PassNC_000007.14Chr763,202,57363,389,022
essv7014713RemappedPassNC_000007.14:g.(?_
61578038)_(6237623
9_?)delNT_187383.1
:g.(?_331112)_(610
898_?)del
GRCh38.p12Second PassNT_187383.1Chr16|NT_1
87383.1
331,112610,898
essv7014714RemappedPassNT_187383.1:g.(?_3
31112)_(610898_?)d
upNC_000007.14:g.(
?_61578038)_(62376
239_?)dup
GRCh38.p12Second PassNT_187383.1Chr16|NT_1
87383.1
331,112610,898
essv7014715RemappedPassNT_187383.1:g.(?_3
31112)_(610898_?)d
upNC_000007.14:g.(
?_61578038)_(62376
239_?)dup
GRCh38.p12Second PassNT_187383.1Chr16|NT_1
87383.1
331,112610,898
essv7014716RemappedPassNC_000007.14:g.(?_
61578038)_(6237623
9_?)delNT_187383.1
:g.(?_331112)_(610
898_?)del
GRCh38.p12Second PassNT_187383.1Chr16|NT_1
87383.1
331,112610,898
essv7014717RemappedPassNC_000007.14:g.(?_
61578038)_(6237623
9_?)delNT_187383.1
:g.(?_331112)_(610
898_?)del
GRCh38.p12Second PassNT_187383.1Chr16|NT_1
87383.1
331,112610,898
essv7014737RemappedPassNT_187383.1:g.(?_3
31112)_(610898_?)d
el
GRCh38.p12Second PassNT_187383.1Chr16|NT_1
87383.1
331,112610,898
essv7014712RemappedPassNC_000007.13:g.(?_
61063974)_(6188812
8_?)dup
GRCh37.p13First PassNC_000007.13Chr761,063,97461,888,128
essv7014713RemappedPassNC_000007.13:g.(?_
61255393)_(6188812
8_?)del
GRCh37.p13First PassNC_000007.13Chr761,255,39361,888,128
essv7014714RemappedPassNC_000007.13:g.(?_
61255393)_(6188812
8_?)dup
GRCh37.p13First PassNC_000007.13Chr761,255,39361,888,128
essv7014715RemappedPassNC_000007.13:g.(?_
61255393)_(6188812
8_?)dup
GRCh37.p13First PassNC_000007.13Chr761,255,39361,888,128
essv7014716RemappedPassNC_000007.13:g.(?_
61288820)_(6188812
8_?)del
GRCh37.p13First PassNC_000007.13Chr761,288,82061,888,128
essv7014717RemappedPassNC_000007.13:g.(?_
61307080)_(6188812
8_?)del
GRCh37.p13First PassNC_000007.13Chr761,307,08061,888,128
essv7014718RemappedPerfectNC_000007.13:g.(?_
61728407)_(6185118
7_?)del
GRCh37.p13First PassNC_000007.13Chr761,728,40761,851,187
essv7014719RemappedPerfectNC_000007.13:g.(?_
61728407)_(6185118
7_?)del
GRCh37.p13First PassNC_000007.13Chr761,728,40761,851,187
essv7014720RemappedPerfectNC_000007.13:g.(?_
61728407)_(6188812
8_?)del
GRCh37.p13First PassNC_000007.13Chr761,728,40761,888,128
essv7014721RemappedPerfectNC_000007.13:g.(?_
61728407)_(6188812
8_?)del
GRCh37.p13First PassNC_000007.13Chr761,728,40761,888,128
essv7014723RemappedPerfectNC_000007.13:g.(?_
61760703)_(6188812
8_?)del
GRCh37.p13First PassNC_000007.13Chr761,760,70361,888,128
essv7014724RemappedPerfectNC_000007.13:g.(?_
61760703)_(6188812
8_?)del
GRCh37.p13First PassNC_000007.13Chr761,760,70361,888,128
essv7014725RemappedPerfectNC_000007.13:g.(?_
61768646)_(6188812
8_?)del
GRCh37.p13First PassNC_000007.13Chr761,768,64661,888,128
essv7014726RemappedPerfectNC_000007.13:g.(?_
61768646)_(6188812
8_?)del
GRCh37.p13First PassNC_000007.13Chr761,768,64661,888,128
essv7014727RemappedPerfectNC_000007.13:g.(?_
61807590)_(6185118
7_?)del
GRCh37.p13First PassNC_000007.13Chr761,807,59061,851,187
essv7014728RemappedPerfectNC_000007.13:g.(?_
61807590)_(6188812
8_?)del
GRCh37.p13First PassNC_000007.13Chr761,807,59061,888,128
essv7014729RemappedPerfectNC_000007.13:g.(?_
61807590)_(6188812
8_?)del
GRCh37.p13First PassNC_000007.13Chr761,807,59061,888,128
essv7014730RemappedPerfectNC_000007.13:g.(?_
61807590)_(6243928
1_?)dup
GRCh37.p13First PassNC_000007.13Chr761,807,59062,439,281
essv7014731RemappedPerfectNC_000007.13:g.(?_
61812158)_(6188812
8_?)del
GRCh37.p13First PassNC_000007.13Chr761,812,15861,888,128
essv7014732RemappedPerfectNC_000007.13:g.(?_
61826081)_(6185837
5_?)del
GRCh37.p13First PassNC_000007.13Chr761,826,08161,858,375
essv7014734RemappedPerfectNC_000007.13:g.(?_
61836450)_(6188812
8_?)del
GRCh37.p13First PassNC_000007.13Chr761,836,45061,888,128
essv7014735RemappedPerfectNC_000007.13:g.(?_
61839495)_(6185837
5_?)del
GRCh37.p13First PassNC_000007.13Chr761,839,49561,858,375
essv7014736RemappedPerfectNC_000007.13:g.(?_
61839495)_(6188812
8_?)del
GRCh37.p13First PassNC_000007.13Chr761,839,49561,888,128
essv7014737RemappedPerfectNC_000007.13:g.(?_
61839495)_(6205944
0_?)del
GRCh37.p13First PassNC_000007.13Chr761,839,49562,059,440
essv7014738RemappedPerfectNC_000007.13:g.(?_
61846306)_(6188812
8_?)del
GRCh37.p13First PassNC_000007.13Chr761,846,30661,888,128
essv7014739RemappedPerfectNC_000007.13:g.(?_
61850293)_(6188812
8_?)del
GRCh37.p13First PassNC_000007.13Chr761,850,29361,888,128
essv7014740RemappedPerfectNC_000007.13:g.(?_
61857945)_(6279280
1_?)dup
GRCh37.p13First PassNC_000007.13Chr761,857,94562,792,801
essv7014741RemappedPerfectNC_000007.13:g.(?_
61987173)_(6225248
1_?)dup
GRCh37.p13First PassNC_000007.13Chr761,987,17362,252,481
essv7014742RemappedPerfectNC_000007.13:g.(?_
62116004)_(6216227
4_?)dup
GRCh37.p13First PassNC_000007.13Chr762,116,00462,162,274
essv7014743RemappedPerfectNC_000007.13:g.(?_
62662951)_(6284940
0_?)dup
GRCh37.p13First PassNC_000007.13Chr762,662,95162,849,400
essv7014712Submitted genomicNC_000007.12:g.(?_
61067916)_(6152556
3_?)dup
NCBI36 (hg18)NC_000007.12Chr761,067,91661,525,563
essv7014713Submitted genomicNC_000007.12:g.(?_
61259335)_(6152556
3_?)del
NCBI36 (hg18)NC_000007.12Chr761,259,33561,525,563
essv7014714Submitted genomicNC_000007.12:g.(?_
61259335)_(6152556
3_?)dup
NCBI36 (hg18)NC_000007.12Chr761,259,33561,525,563
essv7014715Submitted genomicNC_000007.12:g.(?_
61259335)_(6152556
3_?)dup
NCBI36 (hg18)NC_000007.12Chr761,259,33561,525,563
essv7014716Submitted genomicNC_000007.12:g.(?_
61292762)_(6152556
3_?)del
NCBI36 (hg18)NC_000007.12Chr761,292,76261,525,563
essv7014717Submitted genomicNC_000007.12:g.(?_
61311022)_(6152556
3_?)del
NCBI36 (hg18)NC_000007.12Chr761,311,02261,525,563
essv7014718Submitted genomicNC_000007.12:g.(?_
61365842)_(6148862
2_?)del
NCBI36 (hg18)NC_000007.12Chr761,365,84261,488,622
essv7014719Submitted genomicNC_000007.12:g.(?_
61365842)_(6148862
2_?)del
NCBI36 (hg18)NC_000007.12Chr761,365,84261,488,622
essv7014720Submitted genomicNC_000007.12:g.(?_
61365842)_(6152556
3_?)del
NCBI36 (hg18)NC_000007.12Chr761,365,84261,525,563
essv7014721Submitted genomicNC_000007.12:g.(?_
61365842)_(6152556
3_?)del
NCBI36 (hg18)NC_000007.12Chr761,365,84261,525,563
essv7014723Submitted genomicNC_000007.12:g.(?_
61398138)_(6152556
3_?)del
NCBI36 (hg18)NC_000007.12Chr761,398,13861,525,563
essv7014724Submitted genomicNC_000007.12:g.(?_
61398138)_(6152556
3_?)del
NCBI36 (hg18)NC_000007.12Chr761,398,13861,525,563
essv7014725Submitted genomicNC_000007.12:g.(?_
61406081)_(6152556
3_?)del
NCBI36 (hg18)NC_000007.12Chr761,406,08161,525,563
essv7014726Submitted genomicNC_000007.12:g.(?_
61406081)_(6152556
3_?)del
NCBI36 (hg18)NC_000007.12Chr761,406,08161,525,563
essv7014727Submitted genomicNC_000007.12:g.(?_
61445025)_(6148862
2_?)del
NCBI36 (hg18)NC_000007.12Chr761,445,02561,488,622
essv7014728Submitted genomicNC_000007.12:g.(?_
61445025)_(6152556
3_?)del
NCBI36 (hg18)NC_000007.12Chr761,445,02561,525,563
essv7014729Submitted genomicNC_000007.12:g.(?_
61445025)_(6152556
3_?)del
NCBI36 (hg18)NC_000007.12Chr761,445,02561,525,563
essv7014730Submitted genomicNC_000007.12:g.(?_
61445025)_(6207671
6_?)dup
NCBI36 (hg18)NC_000007.12Chr761,445,02562,076,716
essv7014731Submitted genomicNC_000007.12:g.(?_
61449593)_(6152556
3_?)del
NCBI36 (hg18)NC_000007.12Chr761,449,59361,525,563
essv7014732Submitted genomicNC_000007.12:g.(?_
61463516)_(6149581
0_?)del
NCBI36 (hg18)NC_000007.12Chr761,463,51661,495,810
essv7014734Submitted genomicNC_000007.12:g.(?_
61473885)_(6152556
3_?)del
NCBI36 (hg18)NC_000007.12Chr761,473,88561,525,563
essv7014735Submitted genomicNC_000007.12:g.(?_
61476930)_(6149581
0_?)del
NCBI36 (hg18)NC_000007.12Chr761,476,93061,495,810
essv7014736Submitted genomicNC_000007.12:g.(?_
61476930)_(6152556
3_?)del
NCBI36 (hg18)NC_000007.12Chr761,476,93061,525,563
essv7014737Submitted genomicNC_000007.12:g.(?_
61476930)_(6169687
5_?)del
NCBI36 (hg18)NC_000007.12Chr761,476,93061,696,875
essv7014738Submitted genomicNC_000007.12:g.(?_
61483741)_(6152556
3_?)del
NCBI36 (hg18)NC_000007.12Chr761,483,74161,525,563
essv7014739Submitted genomicNC_000007.12:g.(?_
61487728)_(6152556
3_?)del
NCBI36 (hg18)NC_000007.12Chr761,487,72861,525,563
essv7014740Submitted genomicNC_000007.12:g.(?_
61495380)_(6243023
6_?)dup
NCBI36 (hg18)NC_000007.12Chr761,495,38062,430,236
essv7014741Submitted genomicNC_000007.12:g.(?_
61624608)_(6188991
6_?)dup
NCBI36 (hg18)NC_000007.12Chr761,624,60861,889,916
essv7014742Submitted genomicNC_000007.12:g.(?_
61753439)_(6179970
9_?)dup
NCBI36 (hg18)NC_000007.12Chr761,753,43961,799,709
essv7014743Submitted genomicNC_000007.12:g.(?_
62300386)_(6248683
5_?)dup
NCBI36 (hg18)NC_000007.12Chr762,300,38662,486,835

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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