A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5881654



Internal ID9483662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:71835730..71837190hg38UCSC Ensembl
Outerchr8:71835693..71837240hg38UCSC Ensembl
Innerchr8:72747965..72749425hg19UCSC Ensembl
Outerchr8:72747928..72749475hg19UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg381548
hg191548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2660712
Supporting Variants
SamplesNA18953
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5881654
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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