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nsv7060637

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,256

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 89 SVs from 16 studies. See in: genome view    
    Submitted genomic76,033,142-76,038,397Question Mark
    Overlapping variant regions from other studies: 89 SVs from 16 studies. See in: genome view    
    Remapped(Score: Perfect):77,792,900-77,798,155Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7060637Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1076,033,14276,038,397
    nsv7060637RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1077,792,90077,798,155

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18736764inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18736764Submitted genomicNC_000010.11:g.760
    33142_76038397inv
    GRCh38 (hg38)NC_000010.11Chr1076,033,14276,038,397
    nssv18736764RemappedPerfectNC_000010.10:g.777
    92900_77798155inv
    GRCh37.p13First PassNC_000010.10Chr1077,792,90077,798,155

    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)
    nssv187367644e-061276268
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