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nsv6891843

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:47,159

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 201 SVs from 39 studies. See in: genome view    
    Submitted genomic101,586,386-101,633,544Question Mark
    Overlapping variant regions from other studies: 201 SVs from 39 studies. See in: genome view    
    Remapped(Score: Perfect):103,346,143-103,393,301Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6891843Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr10101,586,386101,633,544
    nsv6891843RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr10103,346,143103,393,301

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18581529duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18581529Submitted genomicNC_000010.11:g.101
    586386_101633544du
    p
    GRCh38 (hg38)NC_000010.11Chr10101,586,386101,633,544
    nssv18581529RemappedPerfectNC_000010.10:g.103
    346143_103393301du
    p
    GRCh37.p13First PassNC_000010.10Chr10103,346,143103,393,301

    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)
    nssv185815294e-061257178
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