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nsv6832416

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:35,400

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 199 SVs from 43 studies. See in: genome view    
    Submitted genomic77,699,501-77,734,900Question Mark
    Overlapping variant regions from other studies: 200 SVs from 44 studies. See in: genome view    
    Remapped(Score: Perfect):77,328,818-77,364,217Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6832416Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr777,699,50177,734,900
    nsv6832416RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr777,328,81877,364,217

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18728279duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18728279Submitted genomicNC_000007.14:g.776
    99501_77734900dup
    GRCh38 (hg38)NC_000007.14Chr777,699,50177,734,900
    nssv18728279RemappedPerfectNC_000007.13:g.773
    28818_77364217dup
    GRCh37.p13First PassNC_000007.13Chr777,328,81877,364,217

    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)
    nssv187282791.4e-054274220
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