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nsv6880020

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,574

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 192 SVs from 36 studies. See in: genome view    
    Submitted genomic48,273,340-48,279,913Question Mark
    Overlapping variant regions from other studies: 190 SVs from 36 studies. See in: genome view    
    Remapped(Score: Perfect):49,481,383-49,487,956Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6880020Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1048,273,34048,279,913
    nsv6880020RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1049,481,38349,487,956

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18336710deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18336710Submitted genomicNC_000010.11:g.482
    73340_48279913del
    GRCh38 (hg38)NC_000010.11Chr1048,273,34048,279,913
    nssv18336710RemappedPerfectNC_000010.10:g.494
    81383_49487956del
    GRCh37.p13First PassNC_000010.10Chr1049,481,38349,487,956

    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)
    nssv183367104e-061276220
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