A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5512701



Internal ID289250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:34068749..34068884hg38UCSC Ensembl
chr11:34090296..34090431hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17046039
Samples
Known GenesCAPRIN1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5512701
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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