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nsv6523086

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,393

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 100 SVs from 28 studies. See in: genome view    
    Submitted genomic49,549,921-49,554,313Question Mark
    Overlapping variant regions from other studies: 100 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):50,053,178-50,057,570Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6523086Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1949,549,92149,554,313
    nsv6523086RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1950,053,17850,057,570

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18047179deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18047179Submitted genomicNC_000019.10:g.495
    49921_49554313del
    GRCh38 (hg38)NC_000019.10Chr1949,549,92149,554,313
    nssv18047179RemappedPerfectNC_000019.9:g.5005
    3178_50057570del
    GRCh37.p13First PassNC_000019.9Chr1950,053,17850,057,570

    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)
    nssv18047179<0.001138886
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