A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8689811



Internal ID14708454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:84219996..84223094hg38UCSC Ensembl
Innerchr15:84220996..84222094hg38UCSC Ensembl
Outerchr15:84218996..84224094hg38UCSC Ensembl
chr15:84888748..84891846hg19UCSC Ensembl
Innerchr15:84889748..84890846hg19UCSC Ensembl
Outerchr15:84887748..84892846hg19UCSC Ensembl
chr15:82679752..82682850hg18UCSC Ensembl
Innerchr15:82680752..82681850hg18UCSC Ensembl
Outerchr15:82678752..82683850hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg383099
hg193099
hg183099
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3329086
Supporting Variants
SamplesNA19239
Known GenesLOC388152
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8689811
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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