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nsv823628

  • Variant Calls:3
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,495

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 925 SVs from 69 studies. See in: genome view    
Remapped(Score: Perfect):32,644,291-32,645,785Question Mark
Overlapping variant regions from other studies: 366 SVs from 30 studies. See in: genome view    
Remapped(Score: Pass):3,945,317-3,946,695Question Mark
Overlapping variant regions from other studies: 354 SVs from 30 studies. See in: genome view    
Remapped(Score: Pass):4,046,186-4,047,564Question Mark
Overlapping variant regions from other studies: 244 SVs from 28 studies. See in: genome view    
Remapped(Score: Pass):4,062,538-4,063,916Question Mark
Overlapping variant regions from other studies: 402 SVs from 25 studies. See in: genome view    
Remapped(Score: Pass):3,888,140-3,889,518Question Mark
Overlapping variant regions from other studies: 925 SVs from 69 studies. See in: genome view    
Remapped(Score: Perfect):32,612,068-32,613,562Question Mark
Overlapping variant regions from other studies: 416 SVs from 26 studies. See in: genome view    
Remapped(Score: Pass):3,893,725-3,895,103Question Mark
Overlapping variant regions from other studies: 366 SVs from 30 studies. See in: genome view    
Remapped(Score: Pass):3,950,902-3,952,277Question Mark
Overlapping variant regions from other studies: 477 SVs from 30 studies. See in: genome view    
Remapped(Score: Pass):4,045,484-4,046,862Question Mark
Overlapping variant regions from other studies: 244 SVs from 28 studies. See in: genome view    
Remapped(Score: Pass):4,068,158-4,069,536Question Mark
Overlapping variant regions from other studies: 653 SVs from 25 studies. See in: genome view    
Submitted genomic32,720,046-32,721,540Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv823628RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr632,644,29132,645,785
nsv823628RemappedPassGRCh38.p12ALT_REF_LOCI_5Second PassNT_167247.2Chr6|NT_16
7247.2		3,945,3173,946,695
nsv823628RemappedPassGRCh38.p12ALT_REF_LOCI_7Second PassNT_167249.2Chr6|NT_16
7249.2		4,046,1864,047,564
nsv823628RemappedPassGRCh38.p12ALT_REF_LOCI_4Second PassNT_167246.2Chr6|NT_16
7246.2		4,062,5384,063,916
nsv823628RemappedPassGRCh38.p12ALT_REF_LOCI_3Second PassNT_167245.2Chr6|NT_16
7245.2		3,888,1403,889,518
nsv823628RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr632,612,06832,613,562
nsv823628RemappedPassGRCh37.p13ALT_REF_LOCI_3Second PassNT_167245.1Chr6|NT_16
7245.1		3,893,7253,895,103
nsv823628RemappedPassGRCh37.p13ALT_REF_LOCI_5Second PassNT_167247.1Chr6|NT_16
7247.1		3,950,9023,952,277
nsv823628RemappedPassGRCh37.p13ALT_REF_LOCI_7Second PassNT_167249.1Chr6|NT_16
7249.1		4,045,4844,046,862
nsv823628RemappedPassGRCh37.p13ALT_REF_LOCI_4Second PassNT_167246.1Chr6|NT_16
7246.1		4,068,1584,069,536
nsv823628Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000006.10Chr632,720,04632,721,540

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv1432089copy number lossAK20Oligo aCGHProbe signal intensity768
nssv1435902copy number gainNA18566Oligo aCGHProbe signal intensity605
nssv1438869copy number lossNA18973Oligo aCGHProbe signal intensity782

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv1432089RemappedPassNT_167247.2:g.(?_3
945317)_(3946695_?
)del		GRCh38.p12Second PassNT_167247.2Chr6|NT_16
7247.2		3,945,3173,946,695
nssv1435902RemappedPassNT_167247.2:g.(?_3
945317)_(3946695_?
)dup		GRCh38.p12Second PassNT_167247.2Chr6|NT_16
7247.2		3,945,3173,946,695
nssv1438869RemappedPassNT_167247.2:g.(?_3
945317)_(3946695_?
)del		GRCh38.p12Second PassNT_167247.2Chr6|NT_16
7247.2		3,945,3173,946,695
nssv1432089RemappedPassNT_167249.2:g.(?_4
046186)_(4047564_?
)del		GRCh38.p12Second PassNT_167249.2Chr6|NT_16
7249.2		4,046,1864,047,564
nssv1435902RemappedPassNT_167249.2:g.(?_4
046186)_(4047564_?
)dup		GRCh38.p12Second PassNT_167249.2Chr6|NT_16
7249.2		4,046,1864,047,564
nssv1438869RemappedPassNT_167249.2:g.(?_4
046186)_(4047564_?
)del		GRCh38.p12Second PassNT_167249.2Chr6|NT_16
7249.2		4,046,1864,047,564
nssv1432089RemappedPassNT_167246.2:g.(?_4
062538)_(4063916_?
)del		GRCh38.p12Second PassNT_167246.2Chr6|NT_16
7246.2		4,062,5384,063,916
nssv1435902RemappedPassNT_167246.2:g.(?_4
062538)_(4063916_?
)dup		GRCh38.p12Second PassNT_167246.2Chr6|NT_16
7246.2		4,062,5384,063,916
nssv1438869RemappedPassNT_167246.2:g.(?_4
062538)_(4063916_?
)del		GRCh38.p12Second PassNT_167246.2Chr6|NT_16
7246.2		4,062,5384,063,916
nssv1432089RemappedPassNT_167245.2:g.(?_3
888140)_(3889518_?
)del		GRCh38.p12Second PassNT_167245.2Chr6|NT_16
7245.2		3,888,1403,889,518
nssv1435902RemappedPassNT_167245.2:g.(?_3
888140)_(3889518_?
)dup		GRCh38.p12Second PassNT_167245.2Chr6|NT_16
7245.2		3,888,1403,889,518
nssv1438869RemappedPassNT_167245.2:g.(?_3
888140)_(3889518_?
)del		GRCh38.p12Second PassNT_167245.2Chr6|NT_16
7245.2		3,888,1403,889,518
nssv1432089RemappedPerfectNC_000006.12:g.(?_
32644291)_(3264578
5_?)del		GRCh38.p12First PassNC_000006.12Chr632,644,29132,645,785
nssv1435902RemappedPerfectNC_000006.12:g.(?_
32644291)_(3264578
5_?)dup		GRCh38.p12First PassNC_000006.12Chr632,644,29132,645,785
nssv1438869RemappedPerfectNC_000006.12:g.(?_
32644291)_(3264578
5_?)del		GRCh38.p12First PassNC_000006.12Chr632,644,29132,645,785
nssv1432089RemappedPassNT_167245.1:g.(?_3
893725)_(3895103_?
)delNT_167245.1:g.
(?_3893725)_(38951
03_?)del		GRCh37.p13Second PassNT_167245.1Chr6|NT_16
7245.1		3,893,7253,895,103
nssv1435902RemappedPassNT_167245.1:g.(?_3
893725)_(3895103_?
)dupNT_167245.1:g.
(?_3893725)_(38951
03_?)dup		GRCh37.p13Second PassNT_167245.1Chr6|NT_16
7245.1		3,893,7253,895,103
nssv1438869RemappedPassNT_167245.1:g.(?_3
893725)_(3895103_?
)delNT_167245.1:g.
(?_3893725)_(38951
03_?)del		GRCh37.p13Second PassNT_167245.1Chr6|NT_16
7245.1		3,893,7253,895,103
nssv1432089RemappedPassNT_167247.1:g.(?_3
950902)_(3952277_?
)delNT_167247.1:g.
(?_3950902)_(39522
77_?)del		GRCh37.p13Second PassNT_167247.1Chr6|NT_16
7247.1		3,950,9023,952,277
nssv1435902RemappedPassNT_167247.1:g.(?_3
950902)_(3952277_?
)dupNT_167247.1:g.
(?_3950902)_(39522
77_?)dup		GRCh37.p13Second PassNT_167247.1Chr6|NT_16
7247.1		3,950,9023,952,277
nssv1438869RemappedPassNT_167247.1:g.(?_3
950902)_(3952277_?
)delNT_167247.1:g.
(?_3950902)_(39522
77_?)del		GRCh37.p13Second PassNT_167247.1Chr6|NT_16
7247.1		3,950,9023,952,277
nssv1432089RemappedPassNT_167249.1:g.(?_4
045484)_(4046862_?
)del		GRCh37.p13Second PassNT_167249.1Chr6|NT_16
7249.1		4,045,4844,046,862
nssv1435902RemappedPassNT_167249.1:g.(?_4
045484)_(4046862_?
)dup		GRCh37.p13Second PassNT_167249.1Chr6|NT_16
7249.1		4,045,4844,046,862
nssv1438869RemappedPassNT_167249.1:g.(?_4
045484)_(4046862_?
)del		GRCh37.p13Second PassNT_167249.1Chr6|NT_16
7249.1		4,045,4844,046,862
nssv1432089RemappedPassNT_167246.1:g.(?_4
068158)_(4069536_?
)delNT_167246.1:g.
(?_4068158)_(40695
36_?)del		GRCh37.p13Second PassNT_167246.1Chr6|NT_16
7246.1		4,068,1584,069,536
nssv1435902RemappedPassNT_167246.1:g.(?_4
068158)_(4069536_?
)dupNT_167246.1:g.
(?_4068158)_(40695
36_?)dup		GRCh37.p13Second PassNT_167246.1Chr6|NT_16
7246.1		4,068,1584,069,536
nssv1438869RemappedPassNT_167246.1:g.(?_4
068158)_(4069536_?
)delNT_167246.1:g.
(?_4068158)_(40695
36_?)del		GRCh37.p13Second PassNT_167246.1Chr6|NT_16
7246.1		4,068,1584,069,536
nssv1432089RemappedPerfectNC_000006.11:g.(?_
32612068)_(3261356
2_?)del		GRCh37.p13First PassNC_000006.11Chr632,612,06832,613,562
nssv1435902RemappedPerfectNC_000006.11:g.(?_
32612068)_(3261356
2_?)dup		GRCh37.p13First PassNC_000006.11Chr632,612,06832,613,562
nssv1438869RemappedPerfectNC_000006.11:g.(?_
32612068)_(3261356
2_?)del		GRCh37.p13First PassNC_000006.11Chr632,612,06832,613,562
nssv1432089Submitted genomicNC_000006.10:g.(?_
32720046)_(3272154
0_?)del		NCBI36 (hg18)NC_000006.10Chr632,720,04632,721,540
nssv1435902Submitted genomicNC_000006.10:g.(?_
32720046)_(3272154
0_?)dup		NCBI36 (hg18)NC_000006.10Chr632,720,04632,721,540
nssv1438869Submitted genomicNC_000006.10:g.(?_
32720046)_(3272154
0_?)del		NCBI36 (hg18)NC_000006.10Chr632,720,04632,721,540

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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