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nsv4086864

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,991

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 40 SVs from 6 studies. See in: genome view    
Remapped(Score: Perfect):218,252,508-218,258,498Question Mark
Overlapping variant regions from other studies: 40 SVs from 6 studies. See in: genome view    
Submitted genomic219,117,231-219,123,221Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4086864RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000002.12Chr2218,252,508218,258,498
nsv4086864Submitted genomicGRCh37.p13Primary AssemblyNC_000002.11Chr2219,117,231219,123,221

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15968191duplicationSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15968191RemappedPerfectNC_000002.12:g.218
252508_218258498du
p
GRCh38.p12First PassNC_000002.12Chr2218,252,508218,258,498
nssv15968191Submitted genomicNC_000002.11:g.219
117231_219123221du
p
GRCh37.p13NC_000002.11Chr2219,117,231219,123,221

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)
nssv15968191<0.001321694
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