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nsv6466380

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,152

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 99 SVs from 35 studies. See in: genome view    
    Submitted genomic64,707,277-64,710,428Question Mark
    Overlapping variant regions from other studies: 99 SVs from 35 studies. See in: genome view    
    Remapped(Score: Perfect):64,474,749-64,477,900Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6466380Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1164,707,27764,710,428
    nsv6466380RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1164,474,74964,477,900

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv17993860deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv17993860Submitted genomicNC_000011.10:g.647
    07277_64710428del
    GRCh38 (hg38)NC_000011.10Chr1164,707,27764,710,428
    nssv17993860RemappedPerfectNC_000011.9:g.6447
    4749_64477900del
    GRCh37.p13First PassNC_000011.9Chr1164,474,74964,477,900

    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)
    nssv17993860<0.001138770
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