A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1804n209



Internal ID22827879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158892891..158898025hg38UCSC Ensembl
chr6:159313923..159319057hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg385135
hg195135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5904477, nsv5894344
Samples
Known GenesC6orf99
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv1804n209
Frequency
Sample Size914
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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