A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16952587



Internal ID35750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:83110693..83110794hg38UCSC Ensembl
chr4:84031846..84031947hg19UCSC Ensembl
Cytoband4q21.22
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5462777
Supporting Variants
Samples
Known GenesPLAC8
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16952587
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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