U.S. flag

An official website of the United States government

nsv5410038

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:101

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 73 SVs from 14 studies. See in: genome view    
Submitted genomic181,659,130-181,659,230Question Mark
Overlapping variant regions from other studies: 73 SVs from 14 studies. See in: genome view    
Remapped(Score: Perfect):181,376,918-181,377,018Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5410038Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3181,659,130181,659,230
nsv5410038RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3181,376,918181,377,018

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16943288alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16943288Submitted genomicNC_000003.12:g.181
659130_181659230in
s279
GRCh38 (hg38)NC_000003.12Chr3181,659,130181,659,230
nssv16943288RemappedPerfectNC_000003.11:g.181
376918_181377018in
s279
GRCh37.p13First PassNC_000003.11Chr3181,376,918181,377,018

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)
nssv16943288<0.00126404
Support Center