A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17684571



Internal ID108237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:113359333..113362417hg38UCSC Ensembl
chr12:113797138..113800222hg19UCSC Ensembl
Cytoband12q24.13
Allele length
AssemblyAllele length
hg383085
hg193085
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5504338
Supporting Variants
Samples
Known GenesPLBD2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17684571
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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