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nsv6996686

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:16,700

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 275 SVs from 40 studies. See in: genome view    
    Submitted genomic75,581,201-75,597,900Question Mark
    Overlapping variant regions from other studies: 275 SVs from 40 studies. See in: genome view    
    Remapped(Score: Perfect):73,577,282-73,593,981Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6996686Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1775,581,20175,597,900
    nsv6996686RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1773,577,28273,593,981

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18631302duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18631302Submitted genomicNC_000017.11:g.755
    81201_75597900dup
    GRCh38 (hg38)NC_000017.11Chr1775,581,20175,597,900
    nssv18631302RemappedPerfectNC_000017.10:g.735
    77282_73593981dup
    GRCh37.p13First PassNC_000017.10Chr1773,577,28273,593,981

    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)
    nssv186313021.1e-053271608
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