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nsv6779359

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:409,760

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1057 SVs from 75 studies. See in: genome view    
    Submitted genomic68,020,803-68,430,562Question Mark
    Overlapping variant regions from other studies: 1057 SVs from 75 studies. See in: genome view    
    Remapped(Score: Perfect):68,730,695-69,140,454Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6779359Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr668,020,80368,430,562
    nsv6779359RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr668,730,69569,140,454

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18714415duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18714415Submitted genomicNC_000006.12:g.680
    20803_68430562dup
    GRCh38 (hg38)NC_000006.12Chr668,020,80368,430,562
    nssv18714415RemappedPerfectNC_000006.11:g.687
    30695_69140454dup
    GRCh37.p13First PassNC_000006.11Chr668,730,69569,140,454

    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)
    nssv187144154e-061273998
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