A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5506008



Internal ID282766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76162728..76189667hg38UCSC Ensembl
chr11:75873772..75900711hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg3826940
hg1926940
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17048522
Samples
Known GenesWNT11
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5506008
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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