A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12668417



Internal ID5660369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2319820..2326699hg38UCSC Ensembl
Innerchr7:2320320..2326199hg38UCSC Ensembl
Outerchr7:2318820..2327699hg38UCSC Ensembl
chr7:2359455..2366334hg19UCSC Ensembl
Innerchr7:2359955..2365834hg19UCSC Ensembl
Outerchr7:2358455..2367334hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg386880
hg196880
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3611838
Supporting Variants
SamplesNA19072
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12668417
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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