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nsv7054580

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:611,753

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1298 SVs from 74 studies. See in: genome view    
    Submitted genomic33,076,956-33,688,708Question Mark
    Overlapping variant regions from other studies: 1298 SVs from 74 studies. See in: genome view    
    Remapped(Score: Perfect):33,542,557-34,154,308Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7054580Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr133,076,95633,688,708
    nsv7054580RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr133,542,55734,154,308

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18760306inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18760306Submitted genomicNC_000001.11:g.330
    76956_33688708inv
    GRCh38 (hg38)NC_000001.11Chr133,076,95633,688,708
    nssv18760306RemappedPerfectNC_000001.10:g.335
    42557_34154308inv
    GRCh37.p13First PassNC_000001.10Chr133,542,55734,154,308

    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)
    nssv187603064e-061276268
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