A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659096



Internal ID9925201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:62863442..62866484hg38UCSC Ensembl
chr18:60530675..60533717hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg383043
hg193043
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6244825
SamplesHG00737
Known GenesPHLPP1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659096
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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