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nsv6753784

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:94

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 134 SVs from 28 studies. See in: genome view    
    Submitted genomic147,624,326-147,624,419Question Mark
    Overlapping variant regions from other studies: 134 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):148,545,477-148,545,570Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6753784Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4147,624,326147,624,419
    nsv6753784RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4148,545,477148,545,570

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18490820deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18490820Submitted genomicNC_000004.12:g.147
    624326_147624419de
    l
    GRCh38 (hg38)NC_000004.12Chr4147,624,326147,624,419
    nssv18490820RemappedPerfectNC_000004.11:g.148
    545477_148545570de
    l
    GRCh37.p13First PassNC_000004.11Chr4148,545,477148,545,570

    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)
    nssv184908200.0082068260050
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