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nsv5460272

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:699

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 102 SVs from 21 studies. See in: genome view    
Submitted genomic65,633,436-65,634,134Question Mark
Overlapping variant regions from other studies: 102 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):64,929,263-64,929,961Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5460272Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr565,633,43665,634,134
nsv5460272RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr564,929,26364,929,961

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16968298deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16968298Submitted genomicNC_000005.10:g.656
33436_65634134del
GRCh38 (hg38)NC_000005.10Chr565,633,43665,634,134
nssv16968298RemappedPerfectNC_000005.9:g.6492
9263_64929961del
GRCh37.p13First PassNC_000005.9Chr564,929,26364,929,961

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)
nssv16968298<0.00126404
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