A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1008871



Internal ID7073734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:24009957..24010690hg38UCSC Ensembl
Innerchr4:24011580..24012313hg19UCSC Ensembl
Innerchr4:23620678..23621411hg18UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38734
hg19734
hg18734
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3587162
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1008871
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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