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nsv4290367

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:100

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 50 SVs from 12 studies. See in: genome view    
Remapped(Score: Perfect):27,221,206-27,221,305Question Mark
Overlapping variant regions from other studies: 50 SVs from 12 studies. See in: genome view    
Submitted genomic27,617,167-27,617,266Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4290367RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000022.11Chr2227,221,20627,221,305
nsv4290367Submitted genomicGRCh37.p13Primary AssemblyNC_000022.10Chr2227,617,16727,617,266

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15864422deletionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15864422RemappedPerfectNC_000022.11:g.272
21206_27221305del
GRCh38.p12First PassNC_000022.11Chr2227,221,20627,221,305
nssv15864422Submitted genomicNC_000022.10:g.276
17167_27617266del
GRCh37.p13NC_000022.10Chr2227,617,16727,617,266

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)
nssv158644220.02757821568
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