A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3587162



Internal ID7058544
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 OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1008871
Supporting Variants
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3587162
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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