U.S. flag

An official website of the United States government

nsv5917513

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:73

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 94 SVs from 26 studies. See in: genome view    
Submitted genomic61,458,185-61,458,257Question Mark
Overlapping variant regions from other studies: 94 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):63,217,943-63,218,015Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5917513Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1061,458,18561,458,257
nsv5917513RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1063,217,94363,218,015

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17358646duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17358646Submitted genomicNC_000010.11:g.614
58185_61458257dup
GRCh38 (hg38)NC_000010.11Chr1061,458,18561,458,257
nssv17358646RemappedPerfectNC_000010.10:g.632
17943_63218015dup
GRCh37.p13First PassNC_000010.10Chr1063,217,94363,218,015

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)
nssv1735864611818
Support Center