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nsv5477382

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:148

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 141 SVs from 24 studies. See in: genome view    
Submitted genomic37,835,319-37,835,466Question Mark
Overlapping variant regions from other studies: 148 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):37,835,316-37,835,463Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5477382Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr937,835,31937,835,466
nsv5477382RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr937,835,31637,835,463

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17024789duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17024789Submitted genomicNC_000009.12:g.378
35319_37835466dup
GRCh38 (hg38)NC_000009.12Chr937,835,31937,835,466
nssv17024789RemappedPerfectNC_000009.11:g.378
35316_37835463dup
GRCh37.p13First PassNC_000009.11Chr937,835,31637,835,463

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)
nssv17024789<0.00126404
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