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nsv6524776

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,237

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 105 SVs from 26 studies. See in: genome view    
    Submitted genomic11,338,936-11,343,172Question Mark
    Overlapping variant regions from other studies: 105 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):11,449,612-11,453,848Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6524776Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1911,338,93611,343,172
    nsv6524776RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1911,449,61211,453,848

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18044999deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18044999Submitted genomicNC_000019.10:g.113
    38936_11343172del
    GRCh38 (hg38)NC_000019.10Chr1911,338,93611,343,172
    nssv18044999RemappedPerfectNC_000019.9:g.1144
    9612_11453848del
    GRCh37.p13First PassNC_000019.9Chr1911,449,61211,453,848

    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)
    nssv18044999<0.001239008
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