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nsv6380027

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:679

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 148 SVs from 31 studies. See in: genome view    
    Submitted genomic70,074,680-70,075,358Question Mark
    Overlapping variant regions from other studies: 148 SVs from 31 studies. See in: genome view    
    Remapped(Score: Perfect):70,940,397-70,941,075Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6380027Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr470,074,68070,075,358
    nsv6380027RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr470,940,39770,941,075

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18119068deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18119068Submitted genomicNC_000004.12:g.700
    74680_70075358del
    GRCh38 (hg38)NC_000004.12Chr470,074,68070,075,358
    nssv18119068RemappedPerfectNC_000004.11:g.709
    40397_70941075del
    GRCh37.p13First PassNC_000004.11Chr470,940,39770,941,075

    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)
    nssv18119068<0.001638138
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