A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586626



Internal ID7058008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:12781664..12891244hg38UCSC Ensembl
Innerchr1:12841807..12951075hg19UCSC Ensembl
Innerchr1:12764394..12873662hg18UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg38109581
hg19109269
hg18109269
Variant TypeCNV gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv990214
Supporting Variants
SamplesHuRef
Known GenesHNRNPCL1, LOC649330, PRAMEF1, PRAMEF11, PRAMEF2, PRAMEF4
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586626
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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