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nsv6454259

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:24,700

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 202 SVs from 38 studies. See in: genome view    
    Submitted genomic84,287,901-84,312,600Question Mark
    Overlapping variant regions from other studies: 202 SVs from 38 studies. See in: genome view    
    Remapped(Score: Perfect):86,047,657-86,072,356Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6454259Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1084,287,90184,312,600
    nsv6454259RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1086,047,65786,072,356

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv17984590deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv17984590Submitted genomicNC_000010.11:g.842
    87901_84312600del
    GRCh38 (hg38)NC_000010.11Chr1084,287,90184,312,600
    nssv17984590RemappedPerfectNC_000010.10:g.860
    47657_86072356del
    GRCh37.p13First PassNC_000010.10Chr1086,047,65786,072,356

    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)
    nssv17984590<0.001139298
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