U.S. flag

An official website of the United States government

nsv5517596

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:203,056

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 786 SVs from 88 studies. See in: genome view    
Submitted genomic20,503,131-20,706,186Question Mark
Overlapping variant regions from other studies: 786 SVs from 88 studies. See in: genome view    
Remapped(Score: Perfect):20,514,453-20,717,508Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5517596Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1620,503,13120,706,186
nsv5517596RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1620,514,45320,717,508

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17706191duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17706191Submitted genomicNC_000016.10:g.205
03131_20706186dup
GRCh38 (hg38)NC_000016.10Chr1620,503,13120,706,186
nssv17706191RemappedPerfectNC_000016.9:g.2051
4453_20717508dup
GRCh37.p13First PassNC_000016.9Chr1620,514,45320,717,508

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)
nssv17706191<0.00116404
Support Center