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nsv6562455

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,494,329

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 6778 SVs from 112 studies. See in: genome view    
    Submitted genomic130,771,234-133,265,562Question Mark
    Overlapping variant regions from other studies: 6778 SVs from 112 studies. See in: genome view    
    Remapped(Score: Perfect):131,692,389-134,186,717Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6562455Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4130,771,234133,265,562
    nsv6562455RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4131,692,389134,186,717

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18263046inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18263046Submitted genomicNC_000004.12:g.130
    771234_133265562in
    v
    GRCh38 (hg38)NC_000004.12Chr4130,771,234133,265,562
    nssv18263046RemappedPerfectNC_000004.11:g.131
    692389_134186717in
    v
    GRCh37.p13First PassNC_000004.11Chr4131,692,389134,186,717

    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)
    nssv18263046<0.0011839254
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