A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663140



Internal ID9582559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:101235341..101237207hg38UCSC Ensembl
chr4:102156498..102158364hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg381867
hg191867
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6436408
SamplesNA19083
Known GenesPPP3CA
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663140
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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