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nsv5542723

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 127 SVs from 27 studies. See in: genome view    
Submitted genomic123,341,892-123,341,892Question Mark
Overlapping variant regions from other studies: 127 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):123,826,439-123,826,439Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5542723Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12123,341,892123,341,892
nsv5542723RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12123,826,439123,826,439

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17690796insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17690796Submitted genomicNC_000012.12:g.123
341892_123341893in
s252
GRCh38 (hg38)NC_000012.12Chr12123,341,892123,341,892
nssv17690796RemappedPerfectNC_000012.11:g.123
826439_123826440in
s252
GRCh37.p13First PassNC_000012.11Chr12123,826,439123,826,439

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)
nssv17690796<0.00116404
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