A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17689288



Internal ID112954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:76783698..76783702hg38UCSC Ensembl
chr12:77177478..77177482hg19UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5535151
Supporting Variants
Samples
Known GenesZDHHC17
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17689288
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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