A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3591462



Internal ID6978790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:82176277..82218169hg38UCSC Ensembl
chr2:82403401..82445293hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3841893
hg1941893
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv710e214
Supporting Variantsessv10561595
SamplesHG02699
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3591462
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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