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nsv6494601

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:140,323

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 880 SVs from 79 studies. See in: genome view    
    Submitted genomic70,079,282-70,219,604Question Mark
    Overlapping variant regions from other studies: 880 SVs from 79 studies. See in: genome view    
    Remapped(Score: Perfect):70,653,414-70,793,736Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6494601Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1370,079,28270,219,604
    nsv6494601RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1370,653,41470,793,736

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18012524deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18012524Submitted genomicNC_000013.11:g.700
    79282_70219604del
    GRCh38 (hg38)NC_000013.11Chr1370,079,28270,219,604
    nssv18012524RemappedPerfectNC_000013.10:g.706
    53414_70793736del
    GRCh37.p13First PassNC_000013.10Chr1370,653,41470,793,736

    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)
    nssv18012524<0.001138502
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