A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3388067



Internal ID15235036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:18033256..18035054hg38UCSC Ensembl
Innerchr3:18034054..18034256hg38UCSC Ensembl
Outerchr3:18032256..18036054hg38UCSC Ensembl
chr3:18074748..18076546hg19UCSC Ensembl
Innerchr3:18075546..18075748hg19UCSC Ensembl
Outerchr3:18073748..18077546hg19UCSC Ensembl
chr3:18049752..18051550hg18UCSC Ensembl
Innerchr3:18050752..18050550hg18UCSC Ensembl
Outerchr3:18048752..18052550hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg381799
hg191799
hg181799
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8693890
SamplesNA19239
Known GenesLOC339862
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3388067
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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