U.S. flag

An official website of the United States government

nsv5437668

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:323,784

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 819 SVs from 68 studies. See in: genome view    
Submitted genomic15,024,690-15,348,473Question Mark
Overlapping variant regions from other studies: 819 SVs from 68 studies. See in: genome view    
Remapped(Score: Perfect):15,164,814-15,488,597Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5437668Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr215,024,69015,348,473
nsv5437668RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr215,164,81415,488,597

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16910108deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16910108Submitted genomicNC_000002.12:g.150
24690_15348473del
GRCh38 (hg38)NC_000002.12Chr215,024,69015,348,473
nssv16910108RemappedPerfectNC_000002.11:g.151
64814_15488597del
GRCh37.p13First PassNC_000002.11Chr215,164,81415,488,597

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)
nssv16910108<0.00126404
Support Center