A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3564852



Internal ID7035952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:84901603..84912889hg38UCSC Ensembl
Outerchr3:84950754..84962040hg19UCSC Ensembl
Outerchr3:85033444..85044730hg18UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3811287
hg1911287
hg1811287
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1009040
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3564852
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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