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nsv5526992

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:99

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 129 SVs from 46 studies. See in: genome view    
Submitted genomic64,371,929-64,372,027Question Mark
Overlapping variant regions from other studies: 129 SVs from 46 studies. See in: genome view    
Remapped(Score: Perfect):64,664,128-64,664,226Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5526992Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1564,371,92964,372,027
nsv5526992RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1564,664,12864,664,226

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17704195deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17704195Submitted genomicNC_000015.10:g.643
71929_64372027del
GRCh38 (hg38)NC_000015.10Chr1564,371,92964,372,027
nssv17704195RemappedPerfectNC_000015.9:g.6466
4128_64664226del
GRCh37.p13First PassNC_000015.9Chr1564,664,12864,664,226

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)
nssv177041950.47930636400
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