A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658388



Internal ID9577807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39912071..39918648hg38UCSC Ensembl
Outerchr8:39911914..39918801hg38UCSC Ensembl
Innerchr8:39769590..39776167hg19UCSC Ensembl
Outerchr8:39769433..39776320hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg386888
hg196888
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6524057
SamplesHG01170
Known GenesIDO1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658388
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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