A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17033844



Internal ID90262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:42067000..42558265hg38UCSC Ensembl
chr10:42596688..43053713hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38491266
hg19457026
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5488943
Supporting Variants
Samples
Known GenesCCNYL2, LINC00839, LOC441666, ZNF37BP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17033844
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00125


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