U.S. flag

An official website of the United States government

nsv6466420

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,086

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 129 SVs from 34 studies. See in: genome view    
    Submitted genomic65,436,492-65,443,577Question Mark
    Overlapping variant regions from other studies: 129 SVs from 34 studies. See in: genome view    
    Remapped(Score: Perfect):65,203,963-65,211,048Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6466420Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1165,436,49265,443,577
    nsv6466420RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1165,203,96365,211,048

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv17994118deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv17994118Submitted genomicNC_000011.10:g.654
    36492_65443577del
    GRCh38 (hg38)NC_000011.10Chr1165,436,49265,443,577
    nssv17994118RemappedPerfectNC_000011.9:g.6520
    3963_65211048del
    GRCh37.p13First PassNC_000011.9Chr1165,203,96365,211,048

    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)
    nssv17994118<0.001339052
    Support Center