A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5495368



Internal ID272485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61662897..61665158hg38UCSC Ensembl
chr11:61430369..61432630hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg382262
hg192262
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17046573
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5495368
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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