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nsv4680248

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,412,186

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 4902 SVs from 108 studies. See in: genome view    
Remapped(Score: Perfect):22,961,804-24,373,989Question Mark
Overlapping variant regions from other studies: 4902 SVs from 108 studies. See in: genome view    
Submitted genomic23,535,943-24,948,127Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv4680248RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000013.11Chr1322,961,80424,373,989
nsv4680248Submitted genomicGRCh37.p13Primary AssemblyNC_000013.10Chr1323,535,94324,948,127

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16211001deletionSNP arraySNP genotyping analysis

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv16211001RemappedPerfectNC_000013.11:g.(?_
22961804)_(2437398
9_?)del
GRCh38.p12First PassNC_000013.11Chr1322,961,80424,373,989
nssv16211001Submitted genomicNC_000013.10:g.(?_
23535943)_(2494812
7_?)del
GRCh37.p13NC_000013.10Chr1323,535,94324,948,127

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call IDAllele Frequency (AF)
nssv16211001<0.001
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