A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1001526



Internal ID7066650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:186292858..186293747hg38UCSC Ensembl
Innerchr4:187214012..187214901hg19UCSC Ensembl
Innerchr4:187451006..187451895hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38890
hg19890
hg18890
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586644
SamplesHuRef
Known GenesF11-AS1
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1001526
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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