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nsv6909314

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,043

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 104 SVs from 24 studies. See in: genome view    
    Submitted genomic34,465,540-34,469,582Question Mark
    Overlapping variant regions from other studies: 104 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):34,487,087-34,491,129Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6909314Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1134,465,54034,469,582
    nsv6909314RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1134,487,08734,491,129

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18349125deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18349125Submitted genomicNC_000011.10:g.344
    65540_34469582del
    GRCh38 (hg38)NC_000011.10Chr1134,465,54034,469,582
    nssv18349125RemappedPerfectNC_000011.9:g.3448
    7087_34491129del
    GRCh37.p13First PassNC_000011.9Chr1134,487,08734,491,129

    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)
    nssv183491254e-061276194
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