A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17702854



Internal ID126520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:63098803..63098940hg38UCSC Ensembl
chr15:63391002..63391139hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5532504
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17702854
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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