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nsv883874

  • Variant Calls:7
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:17,899

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1508 SVs from 93 studies. See in: genome view    
Remapped(Score: Perfect):29,906,838-29,924,659Question Mark
Overlapping variant regions from other studies: 711 SVs from 39 studies. See in: genome view    
Remapped(Score: Good):1,163,172-1,181,070Question Mark
Overlapping variant regions from other studies: 1508 SVs from 93 studies. See in: genome view    
Remapped(Score: Perfect):29,874,615-29,892,436Question Mark
Overlapping variant regions from other studies: 711 SVs from 39 studies. See in: genome view    
Remapped(Score: Good):1,168,792-1,186,690Question Mark
Overlapping variant regions from other studies: 660 SVs from 30 studies. See in: genome view    
Submitted genomic29,982,594-30,000,415Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nsv883874RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr629,906,83829,907,74829,923,64629,924,659
nsv883874RemappedGoodGRCh38.p12ALT_REF_LOCI_4Second PassNT_167246.2Chr6|NT_16
7246.2
1,163,1721,163,1721,181,0701,181,070
nsv883874RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr629,874,61529,875,52529,891,42329,892,436
nsv883874RemappedGoodGRCh37.p13ALT_REF_LOCI_4Second PassNT_167246.1Chr6|NT_16
7246.1
1,168,7921,168,7921,186,6901,186,690
nsv883874Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000006.10Chr629,982,59429,983,50429,999,40230,000,415

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv1564076copy number lossIS30160SNP arraySNP genotyping analysis7
nssv1565389copy number lossIS30409SNP arraySNP genotyping analysis21
nssv1566834copy number lossIS30934SNP arraySNP genotyping analysis8
nssv1571671copy number lossIS32775SNP arraySNP genotyping analysis12
nssv1574828copy number lossIS33632SNP arraySNP genotyping analysis13
nssv1574930copy number lossIS33669SNP arraySNP genotyping analysis30
nssv1593729copy number lossIS39509SNP arraySNP genotyping analysis13

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nssv1564076RemappedGoodNT_167246.2:g.(116
3172_1163172)_(118
1070_1181070)del
GRCh38.p12Second PassNT_167246.2Chr6|NT_16
7246.2
1,163,1721,163,1721,181,0701,181,070
nssv1565389RemappedGoodNT_167246.2:g.(116
3172_1163172)_(118
1070_1181070)del
GRCh38.p12Second PassNT_167246.2Chr6|NT_16
7246.2
1,163,1721,163,1721,181,0701,181,070
nssv1566834RemappedGoodNT_167246.2:g.(116
3172_1163172)_(118
1070_1181070)del
GRCh38.p12Second PassNT_167246.2Chr6|NT_16
7246.2
1,163,1721,163,1721,181,0701,181,070
nssv1571671RemappedGoodNT_167246.2:g.(116
3172_1163172)_(118
1070_1181070)del
GRCh38.p12Second PassNT_167246.2Chr6|NT_16
7246.2
1,163,1721,163,1721,181,0701,181,070
nssv1574828RemappedGoodNT_167246.2:g.(116
3172_1163172)_(118
1070_1181070)del
GRCh38.p12Second PassNT_167246.2Chr6|NT_16
7246.2
1,163,1721,163,1721,181,0701,181,070
nssv1574930RemappedGoodNT_167246.2:g.(116
3172_1163172)_(118
1070_1181070)del
GRCh38.p12Second PassNT_167246.2Chr6|NT_16
7246.2
1,163,1721,163,1721,181,0701,181,070
nssv1593729RemappedGoodNT_167246.2:g.(116
3172_1163172)_(118
1070_1181070)del
GRCh38.p12Second PassNT_167246.2Chr6|NT_16
7246.2
1,163,1721,163,1721,181,0701,181,070
nssv1564076RemappedPerfectNC_000006.12:g.(29
906838_29907748)_(
29923646_29924659)
del
GRCh38.p12First PassNC_000006.12Chr629,906,83829,907,74829,923,64629,924,659
nssv1565389RemappedPerfectNC_000006.12:g.(29
906838_29907748)_(
29923646_29924659)
del
GRCh38.p12First PassNC_000006.12Chr629,906,83829,907,74829,923,64629,924,659
nssv1566834RemappedPerfectNC_000006.12:g.(29
906838_29907748)_(
29923646_29924659)
del
GRCh38.p12First PassNC_000006.12Chr629,906,83829,907,74829,923,64629,924,659
nssv1571671RemappedPerfectNC_000006.12:g.(29
906838_29907748)_(
29923646_29924659)
del
GRCh38.p12First PassNC_000006.12Chr629,906,83829,907,74829,923,64629,924,659
nssv1574828RemappedPerfectNC_000006.12:g.(29
906838_29907748)_(
29923646_29924659)
del
GRCh38.p12First PassNC_000006.12Chr629,906,83829,907,74829,923,64629,924,659
nssv1574930RemappedPerfectNC_000006.12:g.(29
906838_29907748)_(
29923646_29924659)
del
GRCh38.p12First PassNC_000006.12Chr629,906,83829,907,74829,923,64629,924,659
nssv1593729RemappedPerfectNC_000006.12:g.(29
906838_29907748)_(
29923646_29924659)
del
GRCh38.p12First PassNC_000006.12Chr629,906,83829,907,74829,923,64629,924,659
nssv1564076RemappedGoodNT_167246.1:g.(116
8792_1168792)_(118
6690_1186690)delNT
_167246.1:g.(11687
92_1168792)_(11866
90_1186690)del
GRCh37.p13Second PassNT_167246.1Chr6|NT_16
7246.1
1,168,7921,168,7921,186,6901,186,690
nssv1565389RemappedGoodNT_167246.1:g.(116
8792_1168792)_(118
6690_1186690)delNT
_167246.1:g.(11687
92_1168792)_(11866
90_1186690)del
GRCh37.p13Second PassNT_167246.1Chr6|NT_16
7246.1
1,168,7921,168,7921,186,6901,186,690
nssv1566834RemappedGoodNT_167246.1:g.(116
8792_1168792)_(118
6690_1186690)delNT
_167246.1:g.(11687
92_1168792)_(11866
90_1186690)del
GRCh37.p13Second PassNT_167246.1Chr6|NT_16
7246.1
1,168,7921,168,7921,186,6901,186,690
nssv1571671RemappedGoodNT_167246.1:g.(116
8792_1168792)_(118
6690_1186690)delNT
_167246.1:g.(11687
92_1168792)_(11866
90_1186690)del
GRCh37.p13Second PassNT_167246.1Chr6|NT_16
7246.1
1,168,7921,168,7921,186,6901,186,690
nssv1574828RemappedGoodNT_167246.1:g.(116
8792_1168792)_(118
6690_1186690)delNT
_167246.1:g.(11687
92_1168792)_(11866
90_1186690)del
GRCh37.p13Second PassNT_167246.1Chr6|NT_16
7246.1
1,168,7921,168,7921,186,6901,186,690
nssv1574930RemappedGoodNT_167246.1:g.(116
8792_1168792)_(118
6690_1186690)delNT
_167246.1:g.(11687
92_1168792)_(11866
90_1186690)del
GRCh37.p13Second PassNT_167246.1Chr6|NT_16
7246.1
1,168,7921,168,7921,186,6901,186,690
nssv1593729RemappedGoodNT_167246.1:g.(116
8792_1168792)_(118
6690_1186690)delNT
_167246.1:g.(11687
92_1168792)_(11866
90_1186690)del
GRCh37.p13Second PassNT_167246.1Chr6|NT_16
7246.1
1,168,7921,168,7921,186,6901,186,690
nssv1564076RemappedPerfectNC_000006.11:g.(29
874615_29875525)_(
29891423_29892436)
del
GRCh37.p13First PassNC_000006.11Chr629,874,61529,875,52529,891,42329,892,436
nssv1565389RemappedPerfectNC_000006.11:g.(29
874615_29875525)_(
29891423_29892436)
del
GRCh37.p13First PassNC_000006.11Chr629,874,61529,875,52529,891,42329,892,436
nssv1566834RemappedPerfectNC_000006.11:g.(29
874615_29875525)_(
29891423_29892436)
del
GRCh37.p13First PassNC_000006.11Chr629,874,61529,875,52529,891,42329,892,436
nssv1571671RemappedPerfectNC_000006.11:g.(29
874615_29875525)_(
29891423_29892436)
del
GRCh37.p13First PassNC_000006.11Chr629,874,61529,875,52529,891,42329,892,436
nssv1574828RemappedPerfectNC_000006.11:g.(29
874615_29875525)_(
29891423_29892436)
del
GRCh37.p13First PassNC_000006.11Chr629,874,61529,875,52529,891,42329,892,436
nssv1574930RemappedPerfectNC_000006.11:g.(29
874615_29875525)_(
29891423_29892436)
del
GRCh37.p13First PassNC_000006.11Chr629,874,61529,875,52529,891,42329,892,436
nssv1593729RemappedPerfectNC_000006.11:g.(29
874615_29875525)_(
29891423_29892436)
del
GRCh37.p13First PassNC_000006.11Chr629,874,61529,875,52529,891,42329,892,436
nssv1564076Submitted genomicNC_000006.10:g.(29
982594_29983504)_(
29999402_30000415)
del
NCBI36 (hg18)NC_000006.10Chr629,982,59429,983,50429,999,40230,000,415
nssv1565389Submitted genomicNC_000006.10:g.(29
982594_29983504)_(
29999402_30000415)
del
NCBI36 (hg18)NC_000006.10Chr629,982,59429,983,50429,999,40230,000,415
nssv1566834Submitted genomicNC_000006.10:g.(29
982594_29983504)_(
29999402_30000415)
del
NCBI36 (hg18)NC_000006.10Chr629,982,59429,983,50429,999,40230,000,415
nssv1571671Submitted genomicNC_000006.10:g.(29
982594_29983504)_(
29999402_30000415)
del
NCBI36 (hg18)NC_000006.10Chr629,982,59429,983,50429,999,40230,000,415
nssv1574828Submitted genomicNC_000006.10:g.(29
982594_29983504)_(
29999402_30000415)
del
NCBI36 (hg18)NC_000006.10Chr629,982,59429,983,50429,999,40230,000,415
nssv1574930Submitted genomicNC_000006.10:g.(29
982594_29983504)_(
29999402_30000415)
del
NCBI36 (hg18)NC_000006.10Chr629,982,59429,983,50429,999,40230,000,415
nssv1593729Submitted genomicNC_000006.10:g.(29
982594_29983504)_(
29999402_30000415)
del
NCBI36 (hg18)NC_000006.10Chr629,982,59429,983,50429,999,40230,000,415

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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