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nsv6489564

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:413

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 153 SVs from 13 studies. See in: genome view    
    Submitted genomic102,369,205-102,369,617Question Mark
    Overlapping variant regions from other studies: 153 SVs from 13 studies. See in: genome view    
    Remapped(Score: Perfect):103,021,555-103,021,967Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6489564Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr13102,369,205102,369,617
    nsv6489564RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr13103,021,555103,021,967

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18006371deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18006371Submitted genomicNC_000013.11:g.102
    369205_102369617de
    l
    GRCh38 (hg38)NC_000013.11Chr13102,369,205102,369,617
    nssv18006371RemappedPerfectNC_000013.10:g.103
    021555_103021967de
    l
    GRCh37.p13First PassNC_000013.10Chr13103,021,555103,021,967

    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)
    nssv180063710.0026737686
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