A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5508965



Internal ID285638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:69250253..69250390hg38UCSC Ensembl
chr11:69017720..69017857hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17047691
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5508965
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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