A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv657n145



Internal ID22813673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:179858981..179863619hg38UCSC Ensembl
chr2:180723708..180728346hg19UCSC Ensembl
Cytoband2q31.3
Allele length
AssemblyAllele length
hg384639
hg194639
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3112201, nsv3112779
Samplessample149, sample289
Known GenesMIR1258, ZNF385B
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv657n145
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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