A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8689550



Internal ID15053926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:20383885..20429183hg38UCSC Ensembl
Innerchr15:20384885..20428183hg38UCSC Ensembl
Outerchr15:20382885..20430183hg38UCSC Ensembl
chr15:20589138..20634436hg19UCSC Ensembl
Innerchr15:20590138..20633436hg19UCSC Ensembl
Outerchr15:20588138..20635436hg19UCSC Ensembl
chr15:18849152..18894450hg18UCSC Ensembl
Innerchr15:18850152..18893450hg18UCSC Ensembl
Outerchr15:18848152..18895450hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3845299
hg1945299
hg1845299
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv3415833
Supporting Variants
SamplesNA19239
Known GenesHERC2P3
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8689550
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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