A curated catalogue of human genomic structural variation




Variant Details

Variant: esv998986



Internal ID1854179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:73647458..73649590hg19UCSC Ensembl
Outerchr15:71434511..71436643hg18UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg192815
hg182815
Variant TypeCNV Insertion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsessv3565790
SamplesHuRef
Known GenesHCN4
Method
Analysis
PlatformSanger Sequencing + Illumina Human1Mv1 BeadChip + Agilent Custom 244K CGH Array + Affymetrix Genome-Wide Human SNP 6.0 Array + NimbleGen 42M CGH Array + Agilent Custom 24M CGH Array
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv998986
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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