A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17704208



Internal ID127874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64551560..64551869hg38UCSC Ensembl
chr15:64843759..64844068hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5517283
Supporting Variants
Samples
Known GenesZNF609
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17704208
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.033729


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