A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5477969



Internal ID8455372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:27505061..27506968hg38UCSC Ensembl
chr10:27793990..27795897hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg381908
hg191908
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2671913
Supporting Variants
SamplesNA18963
Known GenesRAB18
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5477969
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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