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nsv4211304

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,136

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 34 SVs from 11 studies. See in: genome view    
Remapped(Score: Perfect):71,398,623-71,405,758Question Mark
Overlapping variant regions from other studies: 33 SVs from 11 studies. See in: genome view    
Submitted genomic71,109,669-71,116,804Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4211304RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr1171,398,62371,405,758
nsv4211304Submitted genomicGRCh37.p13Primary AssemblyNC_000011.9Chr1171,109,66971,116,804

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15802058deletionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15802058RemappedPerfectNC_000011.10:g.713
98623_71405758del
GRCh38.p12First PassNC_000011.10Chr1171,398,62371,405,758
nssv15802058Submitted genomicNC_000011.9:g.7110
9669_71116804del
GRCh37.p13NC_000011.9Chr1171,109,66971,116,804

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)
nssv158020585.1e-005119474
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