A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5728257



Internal ID9681058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:62508803..62534254hg38UCSC Ensembl
Outerchr2:62508646..62534407hg38UCSC Ensembl
Innerchr2:62735938..62761389hg19UCSC Ensembl
Outerchr2:62735781..62761542hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg3825762
hg1925762
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2657823
Supporting Variants
SamplesNA19431
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5728257
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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