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nsv6804600

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:102,551

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 343 SVs from 44 studies. See in: genome view    
    Submitted genomic112,133,360-112,235,910Question Mark
    Overlapping variant regions from other studies: 343 SVs from 44 studies. See in: genome view    
    Remapped(Score: Good):112,454,562-112,557,111Question Mark
    Overlapping variant regions from other studies: 142 SVs from 16 studies. See in: genome view    
    Remapped(Score: Perfect):130,881-233,431Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6804600Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6112,133,360112,235,910
    nsv6804600RemappedGoodGRCh37.p13Primary AssemblySecond PassNC_000006.11Chr6112,454,562112,557,111
    nsv6804600RemappedPerfectGRCh37.p13PATCHESFirst PassNW_003871062.1Chr6|NW_00
    3871062.1
    130,881233,431

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18709527duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18709527Submitted genomicNC_000006.12:g.112
    133360_112235910du
    p
    GRCh38 (hg38)NC_000006.12Chr6112,133,360112,235,910
    nssv18709527RemappedPerfectNW_003871062.1:g.1
    30881_233431dup
    GRCh37.p13First PassNW_003871062.1Chr6|NW_00
    3871062.1
    130,881233,431
    nssv18709527RemappedGoodNC_000006.11:g.112
    454562_112557111du
    p
    GRCh37.p13Second PassNC_000006.11Chr6112,454,562112,557,111

    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)
    nssv187095277e-062273988
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