A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3349096



Internal ID15196078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:22566387..22568685hg38UCSC Ensembl
Innerchr15:22567387..22567685hg38UCSC Ensembl
Outerchr15:22565387..22569685hg38UCSC Ensembl
chr15:23304411..23306709hg19UCSC Ensembl
Innerchr15:23305411..23305709hg19UCSC Ensembl
Outerchr15:23303411..23307709hg19UCSC Ensembl
chr15:20855852..20858150hg18UCSC Ensembl
Innerchr15:20856852..20857150hg18UCSC Ensembl
Outerchr15:20854852..20859150hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg382299
hg192299
hg182299
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1375e59
Supporting Variantsessv8689674
SamplesNA19239
Known GenesHERC2P2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3349096
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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