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nsv6787483

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:85,729

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 300 SVs from 46 studies. See in: genome view    
    Submitted genomic6,643,045-6,728,773Question Mark
    Overlapping variant regions from other studies: 300 SVs from 46 studies. See in: genome view    
    Remapped(Score: Perfect):6,643,278-6,729,006Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6787483Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr66,643,0456,728,773
    nsv6787483RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr66,643,2786,729,006

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18527348deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18527348Submitted genomicNC_000006.12:g.664
    3045_6728773del
    GRCh38 (hg38)NC_000006.12Chr66,643,0456,728,773
    nssv18527348RemappedPerfectNC_000006.11:g.664
    3278_6729006del
    GRCh37.p13First PassNC_000006.11Chr66,643,2786,729,006

    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)
    nssv185273484e-061276152
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