A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv962e214



Internal ID22756856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:185777773..185784050hg38UCSC Ensembl
chr3:185495561..185501838hg19UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg386278
hg196278
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3598972, esv3598973
SamplesHG03410
Known GenesIGF2BP2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv962e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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