U.S. flag

An official website of the United States government

nsv5443881

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:99

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 91 SVs from 21 studies. See in: genome view    
Submitted genomic131,350,127-131,350,225Question Mark
Overlapping variant regions from other studies: 91 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):131,068,971-131,069,069Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5443881Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3131,350,127131,350,225
nsv5443881RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3131,068,971131,069,069

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16937740duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16937740Submitted genomicNC_000003.12:g.131
350127_131350225du
p
GRCh38 (hg38)NC_000003.12Chr3131,350,127131,350,225
nssv16937740RemappedPerfectNC_000003.11:g.131
068971_131069069du
p
GRCh37.p13First PassNC_000003.11Chr3131,068,971131,069,069

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)
nssv16937740<0.00166404
Support Center