A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586391



Internal ID6711087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:13673122..13676539hg38UCSC Ensembl
Innerchr18:13673121..13676538hg19UCSC Ensembl
Innerchr18:13663121..13666538hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg383418
hg193418
hg183418
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1001818
Supporting Variants
SamplesHuRef
Known GenesFAM210A
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586391
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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