A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8689773



Internal ID15095545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:45026862..45032160hg38UCSC Ensembl
Innerchr15:45027862..45031160hg38UCSC Ensembl
Outerchr15:45025862..45033160hg38UCSC Ensembl
chr15:45319060..45324358hg19UCSC Ensembl
Innerchr15:45320060..45323358hg19UCSC Ensembl
Outerchr15:45318060..45325358hg19UCSC Ensembl
chr15:43106352..43111650hg18UCSC Ensembl
Innerchr15:43107352..43110650hg18UCSC Ensembl
Outerchr15:43105352..43112650hg18UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg385299
hg195299
hg185299
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv3370250
Supporting Variants
SamplesNA19240
Known GenesSORD
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8689773
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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