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nsv6347450

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:558

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 130 SVs from 19 studies. See in: genome view    
    Submitted genomic147,874,343-147,874,900Question Mark
    Overlapping variant regions from other studies: 130 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):148,631,912-148,632,469Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6347450Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2147,874,343147,874,900
    nsv6347450RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2148,631,912148,632,469

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18078766deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18078766Submitted genomicNC_000002.12:g.147
    874343_147874900de
    l
    GRCh38 (hg38)NC_000002.12Chr2147,874,343147,874,900
    nssv18078766RemappedPerfectNC_000002.11:g.148
    631912_148632469de
    l
    GRCh37.p13First PassNC_000002.11Chr2148,631,912148,632,469

    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)
    nssv18078766<0.0012437178
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