A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8689756



Internal ID15021065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:28660365..28664363hg38UCSC Ensembl
Innerchr15:28661365..28663363hg38UCSC Ensembl
Outerchr15:28659365..28665363hg38UCSC Ensembl
chr15:28905511..28909509hg19UCSC Ensembl
Innerchr15:28906511..28908509hg19UCSC Ensembl
Outerchr15:28904511..28910509hg19UCSC Ensembl
chr15:26704552..26708550hg18UCSC Ensembl
Innerchr15:26705552..26707550hg18UCSC Ensembl
Outerchr15:26703552..26709550hg18UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg383999
hg193999
hg183999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3428998
Supporting Variants
SamplesNA19238
Known GenesHERC2P9
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8689756
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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