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nsv6455414

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:588

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 171 SVs from 36 studies. See in: genome view    
    Submitted genomic38,601,762-38,602,349Question Mark
    Overlapping variant regions from other studies: 184 SVs from 38 studies. See in: genome view    
    Remapped(Score: Perfect):38,601,759-38,602,346Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6455414Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr938,601,76238,602,349
    nsv6455414RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr938,601,75938,602,346

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18183342deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18183342Submitted genomicNC_000009.12:g.386
    01762_38602349del
    GRCh38 (hg38)NC_000009.12Chr938,601,76238,602,349
    nssv18183342RemappedPerfectNC_000009.11:g.386
    01759_38602346del
    GRCh37.p13First PassNC_000009.11Chr938,601,75938,602,346

    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)
    nssv18183342<0.001130134
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