A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662603



Internal ID9582022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:28233637..28247734hg38UCSC Ensembl
Outerchr8:28233600..28247784hg38UCSC Ensembl
Innerchr8:28091154..28105251hg19UCSC Ensembl
Outerchr8:28091117..28105301hg19UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg3814185
hg1914185
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6286543
SamplesHG00443
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662603
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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