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nsv6824356

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:18,077

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 152 SVs from 40 studies. See in: genome view    
    Submitted genomic77,712,081-77,730,157Question Mark
    Overlapping variant regions from other studies: 153 SVs from 41 studies. See in: genome view    
    Remapped(Score: Perfect):77,341,398-77,359,474Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6824356Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr777,712,08177,730,157
    nsv6824356RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr777,341,39877,359,474

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18544894deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18544894Submitted genomicNC_000007.14:g.777
    12081_77730157del
    GRCh38 (hg38)NC_000007.14Chr777,712,08177,730,157
    nssv18544894RemappedPerfectNC_000007.13:g.773
    41398_77359474del
    GRCh37.p13First PassNC_000007.13Chr777,341,39877,359,474

    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)
    nssv185448947e-062276244
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