A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5495676



Internal ID272779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76839101..76839191hg38UCSC Ensembl
chr11:76550145..76550235hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17047226
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5495676
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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