A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658392



Internal ID9924497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:36514203..36515974hg38UCSC Ensembl
chr3:36555695..36557466hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg381772
hg191772
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5643232, essv5456762
SamplesNA12400, HG00638
Known GenesSTAC
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658392
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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