U.S. flag

An official website of the United States government

nsv6971301

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:34,541

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 327 SVs from 59 studies. See in: genome view    
    Submitted genomic3,639,521-3,674,061Question Mark
    Overlapping variant regions from other studies: 327 SVs from 59 studies. See in: genome view    
    Remapped(Score: Perfect):3,689,522-3,724,062Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6971301Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr163,639,5213,674,061
    nsv6971301RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr163,689,5223,724,062

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18401931deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18401931Submitted genomicNC_000016.10:g.363
    9521_3674061del
    GRCh38 (hg38)NC_000016.10Chr163,639,5213,674,061
    nssv18401931RemappedPerfectNC_000016.9:g.3689
    522_3724062del
    GRCh37.p13First PassNC_000016.9Chr163,689,5223,724,062

    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)
    nssv184019311.8e-055275998
    Support Center