A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv366n206



Internal ID22755670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:7795625..7797457hg38UCSC Ensembl
chr4:7797352..7799184hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg381833
hg191833
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5446703, nsv5438719
Samples
Known GenesAFAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv366n206
Frequency
Sample Size3202
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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