A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3594708



Internal ID6982028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:235438534..235477166hg38UCSC Ensembl
chr2:236347178..236385810hg19UCSC Ensembl
Cytoband2q37.2
Allele length
AssemblyAllele length
hg3838633
hg1938633
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10883517
SamplesNA21127
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3594708
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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