A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677710



Internal ID9943815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:9844142..9882029hg38UCSC Ensembl
Outerchr8:9844105..9882079hg38UCSC Ensembl
Innerchr8:9701652..9739539hg19UCSC Ensembl
Outerchr8:9701615..9739589hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3837975
hg1937975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5716126
SamplesNA18539
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677710
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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