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nsv6316835

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,747

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 114 SVs from 15 studies. See in: genome view    
    Submitted genomic204,080,368-204,082,114Question Mark
    Overlapping variant regions from other studies: 114 SVs from 15 studies. See in: genome view    
    Remapped(Score: Perfect):204,049,496-204,051,242Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6316835Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1204,080,368204,082,114
    nsv6316835RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1204,049,496204,051,242

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18056999deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18056999Submitted genomicNC_000001.11:g.204
    080368_204082114de
    l
    GRCh38 (hg38)NC_000001.11Chr1204,080,368204,082,114
    nssv18056999RemappedPerfectNC_000001.10:g.204
    049496_204051242de
    l
    GRCh37.p13First PassNC_000001.10Chr1204,049,496204,051,242

    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)
    nssv18056999<0.001139004
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