A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586288



Internal ID6710984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:3180834..3182039hg38UCSC Ensembl
Innerchr1:3097398..3098603hg19UCSC Ensembl
Innerchr1:3087258..3088463hg18UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg381206
hg191206
hg181206
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1001450
Supporting Variants
SamplesHuRef
Known GenesPRDM16
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586288
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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