A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv832n145



Internal ID22813848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:183251100..183256267hg38UCSC Ensembl
chr3:182968888..182974055hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg385168
hg195168
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3111602, nsv3117304
Samplessample141, sample139
Known GenesB3GNT5, MCF2L2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv832n145
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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