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nsv6817660

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,852

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 130 SVs from 29 studies. See in: genome view    
    Submitted genomic135,631,136-135,635,987Question Mark
    Overlapping variant regions from other studies: 130 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):135,952,274-135,957,125Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6817660Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6135,631,136135,635,987
    nsv6817660RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6135,952,274135,957,125

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18523236deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18523236Submitted genomicNC_000006.12:g.135
    631136_135635987de
    l
    GRCh38 (hg38)NC_000006.12Chr6135,631,136135,635,987
    nssv18523236RemappedPerfectNC_000006.11:g.135
    952274_135957125de
    l
    GRCh37.p13First PassNC_000006.11Chr6135,952,274135,957,125

    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)
    nssv185232364e-061275750
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