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nsv6804825

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,500

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 137 SVs from 42 studies. See in: genome view    
    Submitted genomic160,207,501-160,217,000Question Mark
    Overlapping variant regions from other studies: 137 SVs from 42 studies. See in: genome view    
    Remapped(Score: Perfect):160,628,533-160,638,032Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6804825Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6160,207,501160,217,000
    nsv6804825RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6160,628,533160,638,032

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18522245deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18522245Submitted genomicNC_000006.12:g.160
    207501_160217000de
    l
    GRCh38 (hg38)NC_000006.12Chr6160,207,501160,217,000
    nssv18522245RemappedPerfectNC_000006.11:g.160
    628533_160638032de
    l
    GRCh37.p13First PassNC_000006.11Chr6160,628,533160,638,032

    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)
    nssv18522245<0.00148253450
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