A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17046037



Internal ID98481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:34063989..34069382hg38UCSC Ensembl
chr11:34085536..34090929hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg385394
hg195394
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5502899
Supporting Variants
Samples
Known GenesCAPRIN1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17046037
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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