U.S. flag

An official website of the United States government

nsv4271983

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:67

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 31 SVs from 8 studies. See in: genome view    
Remapped(Score: Perfect):5,900,698-5,900,764Question Mark
Overlapping variant regions from other studies: 31 SVs from 8 studies. See in: genome view    
Submitted genomic5,900,709-5,900,775Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4271983RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000019.10Chr195,900,6985,900,764
nsv4271983Submitted genomicGRCh37.p13Primary AssemblyNC_000019.9Chr195,900,7095,900,775

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15842236deletionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15842236RemappedPerfectNC_000019.10:g.590
0698_5900764del
GRCh38.p12First PassNC_000019.10Chr195,900,6985,900,764
nssv15842236Submitted genomicNC_000019.9:g.5900
709_5900775del
GRCh37.p13NC_000019.9Chr195,900,7095,900,775

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)
nssv15842236<0.001321694
Support Center