A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1006796



Internal ID7071888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:4535970..4542029hg38UCSC Ensembl
Innerchr1:4596030..4602089hg19UCSC Ensembl
Innerchr1:4495890..4501949hg18UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg386060
hg196060
hg186060
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586737
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1006796
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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