A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5495116



Internal ID272239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:69743491..69743706hg38UCSC Ensembl
chr11:69558259..69558474hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg38216
hg19216
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17046372
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5495116
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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