A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3564064



Internal ID6688447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:28270893..28280959hg38UCSC Ensembl
Outerchr1:28597404..28607470hg19UCSC Ensembl
Outerchr1:28469991..28480057hg18UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg3810067
hg1910067
hg1810067
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv994212
Supporting Variants
SamplesHuRef
Known GenesSESN2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3564064
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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