U.S. flag

An official website of the United States government

nsv5530731

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:79

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 96 SVs from 19 studies. See in: genome view    
Submitted genomic70,581,051-70,581,129Question Mark
Overlapping variant regions from other studies: 96 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):70,873,390-70,873,468Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5530731Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1570,581,05170,581,129
nsv5530731RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1570,873,39070,873,468

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17702342duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17702342Submitted genomicNC_000015.10:g.705
81051_70581129dup
GRCh38 (hg38)NC_000015.10Chr1570,581,05170,581,129
nssv17702342RemappedPerfectNC_000015.9:g.7087
3390_70873468dup
GRCh37.p13First PassNC_000015.9Chr1570,873,39070,873,468

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)
nssv177023420.00196402
Support Center