A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8689677



Internal ID15054514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:22559987..22564885hg38UCSC Ensembl
Innerchr15:22560987..22563885hg38UCSC Ensembl
Outerchr15:22558987..22565885hg38UCSC Ensembl
chr15:23308211..23313109hg19UCSC Ensembl
Innerchr15:23309211..23312109hg19UCSC Ensembl
Outerchr15:23307211..23314109hg19UCSC Ensembl
chr15:20859652..20864550hg18UCSC Ensembl
Innerchr15:20860652..20863550hg18UCSC Ensembl
Outerchr15:20858652..20865550hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg384899
hg194899
hg184899
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv3373959
Supporting Variants
SamplesNA19239
Known GenesHERC2P2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8689677
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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