A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3592769



Internal ID6980096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:144447625..144481219hg38UCSC Ensembl
chr2:145205192..145238786hg19UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg3833595
hg1933595
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10695748, essv10695747
SamplesNA19355, HG00146
Known GenesZEB2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3592769
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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