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nsv979757

  • Variant Calls:1
  • Validation:Not tested
  • Region Size:28,766

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 185 SVs from 38 studies. See in: genome view    
Remapped(Score: Perfect):38,403,105-38,431,870Question Mark
Overlapping variant regions from other studies: 185 SVs from 38 studies. See in: genome view    
Remapped(Score: Perfect):38,799,110-38,827,875Question Mark
Overlapping variant regions from other studies: 43 SVs from 11 studies. See in: genome view    
Submitted genomic37,129,056-37,157,821Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv979757RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000022.11Chr2238,403,10538,431,870
nsv979757RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000022.10Chr2238,799,11038,827,875
nsv979757Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000022.9Chr2237,129,05637,157,821

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisCopy numberOther Calls in this Sample and Study
nssv2766832duplicationPongo_pygmaeus-KB5406_DorisSequencingRead depth39,403

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv2766832RemappedPerfectNC_000022.11:g.(?_
38403105)_(3843187
0_?)dup
GRCh38.p12First PassNC_000022.11Chr2238,403,10538,431,870
nssv2766832RemappedPerfectNC_000022.10:g.(?_
38799110)_(3882787
5_?)dup
GRCh37.p13First PassNC_000022.10Chr2238,799,11038,827,875
nssv2766832Submitted genomicNC_000022.9:g.(?_3
7129056)_(37157821
_?)dup
NCBI36 (hg18)NC_000022.9Chr2237,129,05637,157,821

No validation data were submitted for this variant

No genotype data were submitted for this variant

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