A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5499006



Internal ID275987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:12042766..12042890hg38UCSC Ensembl
chr11:12064313..12064437hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17042864
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5499006
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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