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nsv5542413

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:46

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 118 SVs from 16 studies. See in: genome view    
Submitted genomic190,059,777-190,059,822Question Mark
Overlapping variant regions from other studies: 118 SVs from 16 studies. See in: genome view    
Remapped(Score: Perfect):190,924,503-190,924,548Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5542413Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2190,059,777190,059,822
nsv5542413RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2190,924,503190,924,548

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16923465insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16923465Submitted genomicNC_000002.12:g.190
059777_190059822in
s52
GRCh38 (hg38)NC_000002.12Chr2190,059,777190,059,822
nssv16923465RemappedPerfectNC_000002.11:g.190
924503_190924548in
s52
GRCh37.p13First PassNC_000002.11Chr2190,924,503190,924,548

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)
nssv16923465<0.00126404
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