A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5441673



Internal ID220136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:39310874..39368783hg38UCSC Ensembl
chr3:39352365..39410274hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3857910
hg1957910
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16931551
Samples
Known GenesCCR8
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5441673
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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