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nsv4146514

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:454,798

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1092 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):161,747,555-162,202,352Question Mark
Overlapping variant regions from other studies: 1092 SVs from 21 studies. See in: genome view    
Submitted genomic162,168,587-162,623,384Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4146514RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr6161,747,555162,202,352
nsv4146514Submitted genomicGRCh37.p13Primary AssemblyNC_000006.11Chr6162,168,587162,623,384

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15914621deletionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15914621RemappedPerfectNC_000006.12:g.161
747555_162202352de
l
GRCh38.p12First PassNC_000006.12Chr6161,747,555162,202,352
nssv15914621Submitted genomicNC_000006.11:g.162
168587_162623384de
l
GRCh37.p13NC_000006.11Chr6162,168,587162,623,384

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)
nssv159146214.6e-005121692
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