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nsv4564408

  • 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: 32 SVs from 3 studies. See in: genome view    
Remapped(Score: Perfect):65,614,163-65,614,163Question Mark
Overlapping variant regions from other studies: 32 SVs from 3 studies. See in: genome view    
Submitted genomic66,526,398-66,526,398Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4564408RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr865,614,16365,614,163
nsv4564408Submitted genomicGRCh37.p13Primary AssemblyNC_000008.10Chr866,526,39866,526,398

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16080628sva insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16080628RemappedPerfectNC_000008.11:g.656
14163_65614164ins1
240
GRCh38.p12First PassNC_000008.11Chr865,614,16365,614,163
nssv16080628Submitted genomicNC_000008.10:g.665
26398_66526399ins1
240
GRCh37.p13NC_000008.10Chr866,526,39866,526,398

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)
nssv16080628<0.001421692
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