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nsv6435624

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:499

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 119 SVs from 29 studies. See in: genome view    
    Submitted genomic26,997,239-26,997,737Question Mark
    Overlapping variant regions from other studies: 119 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):27,018,786-27,019,284Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6435624Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1126,997,23926,997,737
    nsv6435624RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1127,018,78627,019,284

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv17989783deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv17989783Submitted genomicNC_000011.10:g.269
    97239_26997737del
    GRCh38 (hg38)NC_000011.10Chr1126,997,23926,997,737
    nssv17989783RemappedPerfectNC_000011.9:g.2701
    8786_27019284del
    GRCh37.p13First PassNC_000011.9Chr1127,018,78627,019,284

    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)
    nssv17989783<0.001135608
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