A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3590321



Internal ID6977650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:34273752..34313115hg38UCSC Ensembl
chr2:34498819..34538182hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg3839364
hg1939364
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv685e214
Supporting Variantsessv10456289
SamplesHG02885
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3590321
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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