A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8689567



Internal ID15019467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:20482785..20503483hg38UCSC Ensembl
Innerchr15:20483785..20502483hg38UCSC Ensembl
Outerchr15:20481785..20504483hg38UCSC Ensembl
chr15:20688038..20708736hg19UCSC Ensembl
Innerchr15:20689038..20707736hg19UCSC Ensembl
Outerchr15:20687038..20709736hg19UCSC Ensembl
chr15:18948052..18968750hg18UCSC Ensembl
Innerchr15:18949052..18967750hg18UCSC Ensembl
Outerchr15:18947052..18969750hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3820699
hg1920699
hg1820699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag0
Merged StatusS
Merged Variantsesv3361552
Supporting Variants
SamplesNA19238
Known GenesHERC2P3
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8689567
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer