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nsv6452820

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:45,508

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 323 SVs from 50 studies. See in: genome view    
    Submitted genomic87,000,010-87,045,517Question Mark
    Overlapping variant regions from other studies: 323 SVs from 50 studies. See in: genome view    
    Remapped(Score: Perfect):88,759,767-88,805,274Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6452820Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1087,000,01087,045,517
    nsv6452820RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1088,759,76788,805,274

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18190940duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18190940Submitted genomicNC_000010.11:g.870
    00010_87045517dup
    GRCh38 (hg38)NC_000010.11Chr1087,000,01087,045,517
    nssv18190940RemappedPerfectNC_000010.10:g.887
    59767_88805274dup
    GRCh37.p13First PassNC_000010.10Chr1088,759,76788,805,274

    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)
    nssv18190940<0.001139238
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