U.S. flag

An official website of the United States government

nsv5425363

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 189 SVs from 33 studies. See in: genome view    
Submitted genomic15,751,233-15,751,284Question Mark
Overlapping variant regions from other studies: 189 SVs from 33 studies. See in: genome view    
Remapped(Score: Perfect):17,123,552-17,123,603Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5425363Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000021.9Chr2115,751,23315,751,284
nsv5425363RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000021.8Chr2117,123,55217,123,603

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17734114alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17734114Submitted genomicNC_000021.9:g.1575
1233_15751284ins28
1
GRCh38 (hg38)NC_000021.9Chr2115,751,23315,751,284
nssv17734114RemappedPerfectNC_000021.8:g.1712
3552_17123603ins28
1
GRCh37.p13First PassNC_000021.8Chr2117,123,55217,123,603

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)
nssv17734114<0.00116404
Support Center