A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3207268



Internal ID22355690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:66513837..66550543hg38UCSC Ensembl
OuterchrX:65733679..65770385hg19UCSC Ensembl
CytobandXq12
Allele length
AssemblyAllele length
hg3836707
hg1936707
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14268962
SamplesHG00732
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3207268
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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