A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1002236



Internal ID27939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:58560967..58562088hg38UCSC Ensembl
Innerchr15:58853166..58854287hg19UCSC Ensembl
Innerchr15:56640458..56641579hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg381122
hg191122
hg181122
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3587283
SamplesHuRef
Known GenesLIPC
MethodOligo aCGH
Analysis
PlatformNot Submitted
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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