A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586709



Internal ID7058091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:347969..358276hg38UCSC Ensembl
Innerchr1:461061..471368hg19UCSC Ensembl
Innerchr1:450924..461231hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3810308
hg1910308
hg1810308
Variant TypeCNV gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1004360
Supporting Variants
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586709
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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