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nsv5454435

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:61,575

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 627 SVs from 76 studies. See in: genome view    
Submitted genomic32,106,096-32,167,670Question Mark
Overlapping variant regions from other studies: 627 SVs from 76 studies. See in: genome view    
Remapped(Score: Perfect):32,106,202-32,167,776Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5454435Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr532,106,09632,167,670
nsv5454435RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr532,106,20232,167,776

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16963339duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16963339Submitted genomicNC_000005.10:g.321
06096_32167670dup
GRCh38 (hg38)NC_000005.10Chr532,106,09632,167,670
nssv16963339RemappedPerfectNC_000005.9:g.3210
6202_32167776dup
GRCh37.p13First PassNC_000005.9Chr532,106,20232,167,776

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)
nssv169633390.021256404
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