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nsv5559162

  • 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: 93 SVs from 30 studies. See in: genome view    
Submitted genomic95,040,224-95,040,275Question Mark
Overlapping variant regions from other studies: 93 SVs from 30 studies. See in: genome view    
Remapped(Score: Perfect):95,434,000-95,434,051Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5559162Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1295,040,22495,040,275
nsv5559162RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1295,434,00095,434,051

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17684224line1 insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17684224Submitted genomicNC_000012.12:g.950
40224_95040275ins1
151
GRCh38 (hg38)NC_000012.12Chr1295,040,22495,040,275
nssv17684224RemappedPerfectNC_000012.11:g.954
34000_95434051ins1
151
GRCh37.p13First PassNC_000012.11Chr1295,434,00095,434,051

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)
nssv17684224<0.00116404
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