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nsv6846857

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,800

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 193 SVs from 33 studies. See in: genome view    
    Submitted genomic94,760,901-94,768,700Question Mark
    Overlapping variant regions from other studies: 193 SVs from 33 studies. See in: genome view    
    Remapped(Score: Perfect):95,773,129-95,780,928Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6846857Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr894,760,90194,768,700
    nsv6846857RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr895,773,12995,780,928

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18560268deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18560268Submitted genomicNC_000008.11:g.947
    60901_94768700del
    GRCh38 (hg38)NC_000008.11Chr894,760,90194,768,700
    nssv18560268RemappedPerfectNC_000008.10:g.957
    73129_95780928del
    GRCh37.p13First PassNC_000008.10Chr895,773,12995,780,928

    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)
    nssv185602684e-061276250
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