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nsv6896048

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,900

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 98 SVs from 22 studies. See in: genome view    
    Submitted genomic28,528,501-28,534,400Question Mark
    Overlapping variant regions from other studies: 98 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):28,817,430-28,823,329Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6896048Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1028,528,50128,534,400
    nsv6896048RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1028,817,43028,823,329

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18583927duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18583927Submitted genomicNC_000010.11:g.285
    28501_28534400dup
    GRCh38 (hg38)NC_000010.11Chr1028,528,50128,534,400
    nssv18583927RemappedPerfectNC_000010.10:g.288
    17430_28823329dup
    GRCh37.p13First PassNC_000010.10Chr1028,817,43028,823,329

    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)
    nssv185839274e-061273786
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