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nsv5501377

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:184

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 86 SVs from 23 studies. See in: genome view    
Submitted genomic56,489,285-56,489,468Question Mark
Overlapping variant regions from other studies: 88 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):56,256,761-56,256,944Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5501377Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1156,489,28556,489,468
nsv5501377RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1156,256,76156,256,944

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17048215deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17048215Submitted genomicNC_000011.10:g.564
89285_56489468del
GRCh38 (hg38)NC_000011.10Chr1156,489,28556,489,468
nssv17048215RemappedPerfectNC_000011.9:g.5625
6761_56256944del
GRCh37.p13First PassNC_000011.9Chr1156,256,76156,256,944

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)
nssv17048215<0.00116404
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