A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17702900



Internal ID126566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64214447..64214508hg38UCSC Ensembl
chr15:64506646..64506707hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5527073
Supporting Variants
Samples
Known GenesCSNK1G1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17702900
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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