A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3590290



Internal ID6630577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:33491091..33502308hg38UCSC Ensembl
chr2:33716158..33727375hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg3811218
hg1911218
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv684e214
Supporting Variantsessv10451262
SamplesNA18552
Known GenesRASGRP3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3590290
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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