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nsv6882959

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:59

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 69 SVs from 19 studies. See in: genome view    
    Submitted genomic45,130,871-45,130,929Question Mark
    Overlapping variant regions from other studies: 69 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):45,626,319-45,626,377Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6882959Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1045,130,87145,130,929
    nsv6882959RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1045,626,31945,626,377

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18336221deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18336221Submitted genomicNC_000010.11:g.451
    30871_45130929del
    GRCh38 (hg38)NC_000010.11Chr1045,130,87145,130,929
    nssv18336221RemappedPerfectNC_000010.10:g.456
    26319_45626377del
    GRCh37.p13First PassNC_000010.10Chr1045,626,31945,626,377

    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)
    nssv18336221<0.001108243134
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