A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5515756



Internal ID292233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15092454..15154158hg38UCSC Ensembl
chr17:14995771..15057475hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3861705
hg1961705
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17711668
Samples
Known GenesCDRT8
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5515756
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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