A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8689558



Internal ID15053935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:20448585..20455283hg38UCSC Ensembl
Innerchr15:20449585..20454283hg38UCSC Ensembl
Outerchr15:20447585..20456283hg38UCSC Ensembl
chr15:20653838..20660536hg19UCSC Ensembl
Innerchr15:20654838..20659536hg19UCSC Ensembl
Outerchr15:20652838..20661536hg19UCSC Ensembl
chr15:18913852..18920550hg18UCSC Ensembl
Innerchr15:18914852..18919550hg18UCSC Ensembl
Outerchr15:18912852..18921550hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg386699
hg196699
hg186699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag0
Merged StatusS
Merged Variantsesv3416081
Supporting Variants
SamplesNA19239
Known GenesHERC2P3
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8689558
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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