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nsv1343639

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:798,202

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 2100 SVs from 95 studies. See in: genome view    
Remapped(Score: Pass):62,308,236-62,514,699Question Mark
Overlapping variant regions from other studies: 2777 SVs from 101 studies. See in: genome view    
Remapped(Score: Pass):61,578,038-62,376,239Question Mark
Overlapping variant regions from other studies: 1134 SVs from 85 studies. See in: genome view    
Remapped(Score: Pass):62,180,400-62,294,432Question Mark
Overlapping variant regions from other studies: 36 SVs from 14 studies. See in: genome view    
Remapped(Score: Pass):334,948-610,813Question Mark
Overlapping variant regions from other studies: 2630 SVs from 98 studies. See in: genome view    
Remapped(Score: Perfect):61,752,487-61,975,077Question Mark
Overlapping variant regions from other studies: 1048 SVs from 27 studies. See in: genome view    
Submitted genomic61,389,922-61,612,512Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv1343639RemappedPassGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr762,308,23662,514,699
nsv1343639RemappedPassGRCh38.p12Primary AssemblySecond PassNC_000007.14Chr761,578,03862,376,239
nsv1343639RemappedPassGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr762,180,40062,294,432
nsv1343639RemappedPassGRCh38.p12Primary AssemblySecond PassNT_187383.1Chr16|NT_1
87383.1		334,948610,813
nsv1343639RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr761,752,48761,975,077
nsv1343639Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000007.12Chr761,389,92261,612,512

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv8348562copy number lossSNP arrayProbe signal intensity

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv8348562RemappedPassNC_000007.14:g.(?_
61578038)_(6237623
9_?)delNC_000007.1
4:g.(?_62180400)_(
62294432_?)delNT_1
87383.1:g.(?_33494
8)_(610813_?)delNC
_000007.14:g.(?_62
308236)_(62514699_
?)del		GRCh38.p12Second PassNC_000007.14Chr761,578,03862,376,239
nssv8348562RemappedPassNC_000007.14:g.(?_
61578038)_(6237623
9_?)delNC_000007.1
4:g.(?_62180400)_(
62294432_?)delNT_1
87383.1:g.(?_33494
8)_(610813_?)delNC
_000007.14:g.(?_62
308236)_(62514699_
?)del		GRCh38.p12First PassNC_000007.14Chr762,180,40062,294,432
nssv8348562RemappedPassNC_000007.14:g.(?_
61578038)_(6237623
9_?)delNC_000007.1
4:g.(?_62180400)_(
62294432_?)delNT_1
87383.1:g.(?_33494
8)_(610813_?)delNC
_000007.14:g.(?_62
308236)_(62514699_
?)del		GRCh38.p12First PassNC_000007.14Chr762,308,23662,514,699
nssv8348562RemappedPassNC_000007.14:g.(?_
61578038)_(6237623
9_?)delNC_000007.1
4:g.(?_62180400)_(
62294432_?)delNT_1
87383.1:g.(?_33494
8)_(610813_?)delNC
_000007.14:g.(?_62
308236)_(62514699_
?)del		GRCh38.p12Second PassNT_187383.1Chr16|NT_1
87383.1		334,948610,813
nssv8348562RemappedPerfectNC_000007.13:g.(?_
61752487)_(6197507
7_?)del		GRCh37.p13First PassNC_000007.13Chr761,752,48761,975,077
nssv8348562Submitted genomicNC_000007.12:g.(?_
61389922)_(6161251
2_?)del		NCBI36 (hg18)NC_000007.12Chr761,389,92261,612,512

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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