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nsv6333959

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,296

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 137 SVs from 26 studies. See in: genome view    
    Submitted genomic160,993,642-160,996,937Question Mark
    Overlapping variant regions from other studies: 141 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):160,963,432-160,966,727Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6333959Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1160,993,642160,996,937
    nsv6333959RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1160,963,432160,966,727

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18052486deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18052486Submitted genomicNC_000001.11:g.160
    993642_160996937de
    l
    GRCh38 (hg38)NC_000001.11Chr1160,993,642160,996,937
    nssv18052486RemappedPerfectNC_000001.10:g.160
    963432_160966727de
    l
    GRCh37.p13First PassNC_000001.10Chr1160,963,432160,966,727

    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)
    nssv18052486<0.001138770
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