U.S. flag

An official website of the United States government

nsv5512981

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,909

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 183 SVs from 36 studies. See in: genome view    
Submitted genomic31,685,453-31,689,361Question Mark
Overlapping variant regions from other studies: 183 SVs from 36 studies. See in: genome view    
Remapped(Score: Perfect):31,707,001-31,710,909Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5512981Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1131,685,45331,689,361
nsv5512981RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1131,707,00131,710,909

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17044615deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17044615Submitted genomicNC_000011.10:g.316
85453_31689361del
GRCh38 (hg38)NC_000011.10Chr1131,685,45331,689,361
nssv17044615RemappedPerfectNC_000011.9:g.3170
7001_31710909del
GRCh37.p13First PassNC_000011.9Chr1131,707,00131,710,909

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)
nssv17044615<0.00116404
Support Center