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nsv5399879

  • 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: 122 SVs from 14 studies. See in: genome view    
Submitted genomic181,045,577-181,045,628Question Mark
Overlapping variant regions from other studies: 122 SVs from 14 studies. See in: genome view    
Remapped(Score: Perfect):181,910,304-181,910,355Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5399879Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2181,045,577181,045,628
nsv5399879RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2181,910,304181,910,355

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16927388alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16927388Submitted genomicNC_000002.12:g.181
045577_181045628in
s280
GRCh38 (hg38)NC_000002.12Chr2181,045,577181,045,628
nssv16927388RemappedPerfectNC_000002.11:g.181
910304_181910355in
s280
GRCh37.p13First PassNC_000002.11Chr2181,910,304181,910,355

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)
nssv16927388<0.00116404
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