A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6063402



Internal ID9040805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:51818710..51819039hg38UCSC Ensembl
chr10:53578470..53578799hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2676165
Supporting Variants
SamplesNA18638
Known GenesPRKG1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6063402
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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