A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5499359



Internal ID276333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119649333..119652481hg38UCSC Ensembl
chr11:119520043..119523191hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg383149
hg193149
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17052278
Samples
Known GenesPVRL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5499359
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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