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nsv6618795

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:476

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 123 SVs from 24 studies. See in: genome view    
    Submitted genomic16,563,107-16,563,582Question Mark
    Overlapping variant regions from other studies: 123 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):16,602,732-16,603,207Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6618795Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr716,563,10716,563,582
    nsv6618795RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr716,602,73216,603,207

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18152307deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18152307Submitted genomicNC_000007.14:g.165
    63107_16563582del
    GRCh38 (hg38)NC_000007.14Chr716,563,10716,563,582
    nssv18152307RemappedPerfectNC_000007.13:g.166
    02732_16603207del
    GRCh37.p13First PassNC_000007.13Chr716,602,73216,603,207

    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)
    nssv181523070.0025937976
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