A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668055



Internal ID9934160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:29066090..29066699hg38UCSC Ensembl
chr8:28923607..28924216hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38610
hg19610
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6173263, essv6550592
SamplesNA18523, NA19436
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668055
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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