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nsv6570050

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,535,376

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 23734 SVs from 126 studies. See in: genome view    
    Submitted genomic169,780,525-178,315,900Question Mark
    Overlapping variant regions from other studies: 23738 SVs from 126 studies. See in: genome view    
    Remapped(Score: Perfect):170,701,676-179,237,054Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6570050Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4169,780,525178,315,900
    nsv6570050RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4170,701,676179,237,054

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18264397inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18264397Submitted genomicNC_000004.12:g.169
    780525_178315900in
    v
    GRCh38 (hg38)NC_000004.12Chr4169,780,525178,315,900
    nssv18264397RemappedPerfectNC_000004.11:g.170
    701676_179237054in
    v
    GRCh37.p13First PassNC_000004.11Chr4170,701,676179,237,054

    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)
    nssv18264397<0.001139304
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