A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14360652



Internal ID22287047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:116797649..116802973hg38UCSC Ensembl
chr11:116668365..116673689hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg385325
hg195325
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3219175
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14360652
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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