A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5501648



Internal ID278541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94882626..94882823hg38UCSC Ensembl
chr11:94615791..94615988hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38198
hg19198
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17050009
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5501648
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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