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nsv5457900

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:65

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 275 SVs from 60 studies. See in: genome view    
Submitted genomic32,162,109-32,162,173Question Mark
Overlapping variant regions from other studies: 275 SVs from 60 studies. See in: genome view    
Remapped(Score: Perfect):32,162,215-32,162,279Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5457900Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr532,162,10932,162,173
nsv5457900RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr532,162,21532,162,279

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16963351deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16963351Submitted genomicNC_000005.10:g.321
62109_32162173del
GRCh38 (hg38)NC_000005.10Chr532,162,10932,162,173
nssv16963351RemappedPerfectNC_000005.9:g.3216
2215_32162279del
GRCh37.p13First PassNC_000005.9Chr532,162,21532,162,279

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)
nssv16963351<0.00126404
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