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nsv4485086

  • 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: 70 SVs from 5 studies. See in: genome view    
Remapped(Score: Perfect):142,739,032-142,739,032Question Mark
Overlapping variant regions from other studies: 69 SVs from 5 studies. See in: genome view    
Submitted genomic143,820,450-143,820,450Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4485086RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr8142,739,032142,739,032
nsv4485086Submitted genomicGRCh37.p13Primary AssemblyNC_000008.10Chr8143,820,450143,820,450

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16084443alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16084443RemappedPerfectNC_000008.11:g.142
739032_142739033in
s280
GRCh38.p12First PassNC_000008.11Chr8142,739,032142,739,032
nssv16084443Submitted genomicNC_000008.10:g.143
820450_143820451in
s280
GRCh37.p13NC_000008.10Chr8143,820,450143,820,450

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)
nssv160844434.6e-005121694
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