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nsv5502908

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:412,762

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1266 SVs from 70 studies. See in: genome view    
Submitted genomic103,839,368-104,252,129Question Mark
Overlapping variant regions from other studies: 1266 SVs from 70 studies. See in: genome view    
Remapped(Score: Perfect):104,491,718-104,904,479Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5502908Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr13103,839,368104,252,129
nsv5502908RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr13104,491,718104,904,479

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17694565duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17694565Submitted genomicNC_000013.11:g.103
839368_104252129du
p
GRCh38 (hg38)NC_000013.11Chr13103,839,368104,252,129
nssv17694565RemappedPerfectNC_000013.10:g.104
491718_104904479du
p
GRCh37.p13First PassNC_000013.10Chr13104,491,718104,904,479

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv17694565<0.00126404
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