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nsv6408578

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:751

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 83 SVs from 15 studies. See in: genome view    
    Submitted genomic148,461,703-148,462,453Question Mark
    Overlapping variant regions from other studies: 83 SVs from 15 studies. See in: genome view    
    Remapped(Score: Perfect):147,841,266-147,842,016Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6408578Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5148,461,703148,462,453
    nsv6408578RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5147,841,266147,842,016

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18125941deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18125941Submitted genomicNC_000005.10:g.148
    461703_148462453de
    l
    GRCh38 (hg38)NC_000005.10Chr5148,461,703148,462,453
    nssv18125941RemappedPerfectNC_000005.9:g.1478
    41266_147842016del
    GRCh37.p13First PassNC_000005.9Chr5147,841,266147,842,016

    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)
    nssv18125941<0.0013138204
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