A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5934758



Internal ID9710686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:196199732..196201511hg38UCSC Ensembl
chr3:195926603..195928382hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg381780
hg191780
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2662732
Supporting Variants
SamplesNA19462
Known GenesZDHHC19
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5934758
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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