A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586578



Internal ID7057960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:192672086..192674257hg38UCSC Ensembl
Innerchr3:192389875..192392046hg19UCSC Ensembl
Innerchr3:193872569..193874740hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg382172
hg192172
hg182172
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv998286
Supporting Variants
SamplesHuRef
Known GenesFGF12
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586578
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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