U.S. flag

An official website of the United States government

nsv5464896

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:269,001

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 922 SVs from 74 studies. See in: genome view    
Submitted genomic133,998,360-134,267,360Question Mark
Overlapping variant regions from other studies: 922 SVs from 74 studies. See in: genome view    
Remapped(Score: Perfect):134,919,515-135,188,515Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5464896Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4133,998,360134,267,360
nsv5464896RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4134,919,515135,188,515

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16957874deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16957874Submitted genomicNC_000004.12:g.133
998360_134267360de
l
GRCh38 (hg38)NC_000004.12Chr4133,998,360134,267,360
nssv16957874RemappedPerfectNC_000004.11:g.134
919515_135188515de
l
GRCh37.p13First PassNC_000004.11Chr4134,919,515135,188,515

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)
nssv16957874<0.00136404
Support Center