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nsv6606071

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:617

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 95 SVs from 22 studies. See in: genome view    
    Submitted genomic120,964,710-120,965,326Question Mark
    Overlapping variant regions from other studies: 95 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):120,604,764-120,605,380Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6606071Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7120,964,710120,965,326
    nsv6606071RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7120,604,764120,605,380

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18151154deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18151154Submitted genomicNC_000007.14:g.120
    964710_120965326de
    l
    GRCh38 (hg38)NC_000007.14Chr7120,964,710120,965,326
    nssv18151154RemappedPerfectNC_000007.13:g.120
    604764_120605380de
    l
    GRCh37.p13First PassNC_000007.13Chr7120,604,764120,605,380

    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)
    nssv18151154<0.0011037996
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