A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8689702



Internal ID15020593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:22476387..22481685hg38UCSC Ensembl
Innerchr15:22477387..22480685hg38UCSC Ensembl
Outerchr15:22475387..22482685hg38UCSC Ensembl
chr15:23391411..23396709hg19UCSC Ensembl
Innerchr15:23392411..23395709hg19UCSC Ensembl
Outerchr15:23390411..23397709hg19UCSC Ensembl
chr15:20942852..20948150hg18UCSC Ensembl
Innerchr15:20943852..20947150hg18UCSC Ensembl
Outerchr15:20941852..20949150hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg385299
hg195299
hg185299
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3435335
Supporting Variants
SamplesNA19238
Known GenesHERC2P7
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8689702
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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