A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8689755



Internal ID15054876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:28660365..28661863hg38UCSC Ensembl
Innerchr15:28660863..28661365hg38UCSC Ensembl
Outerchr15:28659365..28662863hg38UCSC Ensembl
chr15:28905511..28907009hg19UCSC Ensembl
Innerchr15:28906009..28906511hg19UCSC Ensembl
Outerchr15:28904511..28908009hg19UCSC Ensembl
chr15:26704552..26706050hg18UCSC Ensembl
Innerchr15:26705552..26705050hg18UCSC Ensembl
Outerchr15:26703552..26707050hg18UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg381499
hg191499
hg181499
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3403700
Supporting Variants
SamplesNA19239
Known GenesHERC2P9
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8689755
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