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nsv6607651

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:33,063

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 168 SVs from 28 studies. See in: genome view    
    Submitted genomic116,792,441-116,825,503Question Mark
    Overlapping variant regions from other studies: 168 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):117,113,604-117,146,666Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6607651Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6116,792,441116,825,503
    nsv6607651RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6117,113,604117,146,666

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18137181deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18137181Submitted genomicNC_000006.12:g.116
    792441_116825503de
    l
    GRCh38 (hg38)NC_000006.12Chr6116,792,441116,825,503
    nssv18137181RemappedPerfectNC_000006.11:g.117
    113604_117146666de
    l
    GRCh37.p13First PassNC_000006.11Chr6117,113,604117,146,666

    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)
    nssv18137181<0.001139292
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