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nsv6380377

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:400

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 117 SVs from 29 studies. See in: genome view    
    Submitted genomic102,868,701-102,869,100Question Mark
    Overlapping variant regions from other studies: 117 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):103,789,858-103,790,257Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6380377Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4102,868,701102,869,100
    nsv6380377RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4103,789,858103,790,257

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18107507deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18107507Submitted genomicNC_000004.12:g.102
    868701_102869100de
    l
    GRCh38 (hg38)NC_000004.12Chr4102,868,701102,869,100
    nssv18107507RemappedPerfectNC_000004.11:g.103
    789858_103790257de
    l
    GRCh37.p13First PassNC_000004.11Chr4103,789,858103,790,257

    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)
    nssv181075070.05192238530
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