A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv656n145



Internal ID22813672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:176130783..176132674hg38UCSC Ensembl
chr2:176995511..176997402hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg381892
hg191892
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3110350, nsv3112377
Samplessample62, sample208
Known GenesHOXD8
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv656n145
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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