A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3388253



Internal ID15235221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:22500387..22501985hg38UCSC Ensembl
Innerchr15:22500985..22501387hg38UCSC Ensembl
Outerchr15:22499387..22502985hg38UCSC Ensembl
chr15:23371111..23372709hg19UCSC Ensembl
Innerchr15:23371709..23372111hg19UCSC Ensembl
Outerchr15:23370111..23373709hg19UCSC Ensembl
chr15:20922552..20924150hg18UCSC Ensembl
Innerchr15:20923552..20923150hg18UCSC Ensembl
Outerchr15:20921552..20925150hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg381599
hg191599
hg181599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8689698
SamplesNA19238
Known GenesHERC2P2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3388253
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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