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nsv6562119

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,875,389

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 22359 SVs from 125 studies. See in: genome view    
    Submitted genomic32,527,628-37,403,016Question Mark
    Overlapping variant regions from other studies: 22360 SVs from 125 studies. See in: genome view    
    Remapped(Score: Perfect):32,495,405-37,370,792Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6562119Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr632,527,62837,403,016
    nsv6562119RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr632,495,40537,370,792

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18270586inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18270586Submitted genomicNC_000006.12:g.325
    27628_37403016inv
    GRCh38 (hg38)NC_000006.12Chr632,527,62837,403,016
    nssv18270586RemappedPerfectNC_000006.11:g.324
    95405_37370792inv
    GRCh37.p13First PassNC_000006.11Chr632,495,40537,370,792

    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)
    nssv182705860.0012726074
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