A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670978



Internal ID9937083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:54041892..54042386hg38UCSC Ensembl
Outerchr8:54041855..54042436hg38UCSC Ensembl
Innerchr8:54954452..54954946hg19UCSC Ensembl
Outerchr8:54954415..54954996hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg38582
hg19582
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6517706
SamplesHG01133
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670978
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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