A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv509n206



Internal ID22755813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:61990981..61998001hg38UCSC Ensembl
chr8:62903540..62910560hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg387021
hg197021
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5490399, nsv5488348
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv509n206
Frequency
Sample Size3202
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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