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nsv6961195

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,618

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 151 SVs from 28 studies. See in: genome view    
    Submitted genomic3,242,518-3,245,135Question Mark
    Overlapping variant regions from other studies: 151 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):3,292,518-3,295,135Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6961195Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr163,242,5183,245,135
    nsv6961195RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr163,292,5183,295,135

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18400561deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18400561Submitted genomicNC_000016.10:g.324
    2518_3245135del
    GRCh38 (hg38)NC_000016.10Chr163,242,5183,245,135
    nssv18400561RemappedPerfectNC_000016.9:g.3292
    518_3295135del
    GRCh37.p13First PassNC_000016.9Chr163,292,5183,295,135

    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)
    nssv184005611.4e-054275476
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