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nsv6857518

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:915

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 262 SVs from 42 studies. See in: genome view    
    Submitted genomic11,370,853-11,371,767Question Mark
    Overlapping variant regions from other studies: 262 SVs from 42 studies. See in: genome view    
    Remapped(Score: Perfect):11,228,362-11,229,276Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6857518Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr811,370,85311,371,767
    nsv6857518RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr811,228,36211,229,276

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18548504deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18548504Submitted genomicNC_000008.11:g.113
    70853_11371767del
    GRCh38 (hg38)NC_000008.11Chr811,370,85311,371,767
    nssv18548504RemappedPerfectNC_000008.10:g.112
    28362_11229276del
    GRCh37.p13First PassNC_000008.10Chr811,228,36211,229,276

    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)
    nssv185485040.0153917271430
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