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nsv6732615

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:155,253

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 783 SVs from 76 studies. See in: genome view    
    Submitted genomic8,207,172-8,362,424Question Mark
    Overlapping variant regions from other studies: 783 SVs from 76 studies. See in: genome view    
    Remapped(Score: Perfect):8,208,899-8,364,151Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6732615Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr48,207,1728,362,424
    nsv6732615RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr48,208,8998,364,151

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18500169deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18500169Submitted genomicNC_000004.12:g.820
    7172_8362424del
    GRCh38 (hg38)NC_000004.12Chr48,207,1728,362,424
    nssv18500169RemappedPerfectNC_000004.11:g.820
    8899_8364151del
    GRCh37.p13First PassNC_000004.11Chr48,208,8998,364,151

    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)
    nssv185001697e-062276182
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