A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv359n206



Internal ID22755663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:177286697..177296679hg38UCSC Ensembl
chr3:177004485..177014467hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg389983
hg199983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5436057, nsv5436861
Samples
Known GenesLINC00501
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv359n206
Frequency
Sample Size3202
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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