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nsv5423972

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:127,375

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 486 SVs from 64 studies. See in: genome view    
Submitted genomic155,047,651-155,175,025Question Mark
Overlapping variant regions from other studies: 493 SVs from 65 studies. See in: genome view    
Remapped(Score: Perfect):155,020,127-155,147,501Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5423972Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1155,047,651155,175,025
nsv5423972RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1155,020,127155,147,501

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16890426duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16890426Submitted genomicNC_000001.11:g.155
047651_155175025du
p
GRCh38 (hg38)NC_000001.11Chr1155,047,651155,175,025
nssv16890426RemappedPerfectNC_000001.10:g.155
020127_155147501du
p
GRCh37.p13First PassNC_000001.10Chr1155,020,127155,147,501

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)
nssv16890426<0.00116404
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