A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17711745



Internal ID135411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15960292..15960572hg38UCSC Ensembl
chr17:15863606..15863886hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6146119
Supporting Variants
Samples
Known GenesADORA2B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17711745
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.521081


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