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nsv5477616

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:447

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 106 SVs from 31 studies. See in: genome view    
Submitted genomic52,308,977-52,309,423Question Mark
Overlapping variant regions from other studies: 110 SVs from 31 studies. See in: genome view    
Remapped(Score: Perfect):54,068,737-54,069,183Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5477616Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1052,308,97752,309,423
nsv5477616RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1054,068,73754,069,183

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17034237deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17034237Submitted genomicNC_000010.11:g.523
08977_52309423del
GRCh38 (hg38)NC_000010.11Chr1052,308,97752,309,423
nssv17034237RemappedPerfectNC_000010.10:g.540
68737_54069183del
GRCh37.p13First PassNC_000010.10Chr1054,068,73754,069,183

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)
nssv170342370.0161016404
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