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nsv6509841

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:735

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 111 SVs from 21 studies. See in: genome view    
    Submitted genomic38,311,814-38,312,548Question Mark
    Overlapping variant regions from other studies: 111 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):38,604,015-38,604,749Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6509841Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1538,311,81438,312,548
    nsv6509841RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1538,604,01538,604,749

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18024091deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18024091Submitted genomicNC_000015.10:g.383
    11814_38312548del
    GRCh38 (hg38)NC_000015.10Chr1538,311,81438,312,548
    nssv18024091RemappedPerfectNC_000015.9:g.3860
    4015_38604749del
    GRCh37.p13First PassNC_000015.9Chr1538,604,01538,604,749

    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)
    nssv18024091<0.001838164
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