A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1002236



Internal ID1854495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:58853166..58854287hg19UCSC Ensembl
Innerchr15:56640458..56641579hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg191122
hg181122
Variant TypeCNV Gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsessv3587283
SamplesHuRef
Known GenesLIPC
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)esv1002236
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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