A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671397



Internal ID9590816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:37426021..37428897hg38UCSC Ensembl
Innerchr7:37465624..37468500hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg382877
hg192877
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5992298
SamplesNA12891
Known GenesELMO1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671397
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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