A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8689673



Internal ID15094970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:22559987..22570085hg38UCSC Ensembl
Innerchr15:22560987..22569085hg38UCSC Ensembl
Outerchr15:22558987..22571085hg38UCSC Ensembl
chr15:23303011..23313109hg19UCSC Ensembl
Innerchr15:23304011..23312109hg19UCSC Ensembl
Outerchr15:23302011..23314109hg19UCSC Ensembl
chr15:20854452..20864550hg18UCSC Ensembl
Innerchr15:20855452..20863550hg18UCSC Ensembl
Outerchr15:20853452..20865550hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3810099
hg1910099
hg1810099
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv3369728
Supporting Variants
SamplesNA19240
Known GenesHERC2P2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8689673
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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