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nsv6357179

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,716

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 96 SVs from 29 studies. See in: genome view    
    Submitted genomic44,598,951-44,602,666Question Mark
    Overlapping variant regions from other studies: 96 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):44,640,443-44,644,158Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6357179Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr344,598,95144,602,666
    nsv6357179RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr344,640,44344,644,158

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18100610deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18100610Submitted genomicNC_000003.12:g.445
    98951_44602666del
    GRCh38 (hg38)NC_000003.12Chr344,598,95144,602,666
    nssv18100610RemappedPerfectNC_000003.11:g.446
    40443_44644158del
    GRCh37.p13First PassNC_000003.11Chr344,640,44344,644,158

    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)
    nssv18100610<0.0012339150
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