A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6321n223



Internal ID22809289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:94744856..94925610hg38UCSC Ensembl
chr6:95454574..95635328hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38180755
hg19180755
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6409780, nsv6405000
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6321n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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