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nsv5492108

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:217

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 988 SVs from 77 studies. See in: genome view    
Submitted genomic39,387,162-39,387,378Question Mark
Overlapping variant regions from other studies: 988 SVs from 77 studies. See in: genome view    
Remapped(Score: Perfect):39,244,681-39,244,897Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5492108Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr839,387,16239,387,378
nsv5492108RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr839,244,68139,244,897

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17009598duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17009598Submitted genomicNC_000008.11:g.393
87162_39387378dup
GRCh38 (hg38)NC_000008.11Chr839,387,16239,387,378
nssv17009598RemappedPerfectNC_000008.10:g.392
44681_39244897dup
GRCh37.p13First PassNC_000008.10Chr839,244,68139,244,897

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)
nssv17009598<0.00126404
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