A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1010898



Internal ID6722989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:36350188..36356123hg38UCSC Ensembl
Innerchr19:36841090..36847025hg19UCSC Ensembl
Innerchr19:41532930..41538865hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg385936
hg195936
hg185936
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586685
SamplesHuRef
Known GenesZFP14
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1010898
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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