A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6753927



Internal ID10162643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:38326492..38327283hg38UCSC Ensembl
Outerchr3:38367983..38368774hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg38792
hg19792
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2725162
Supporting Variants
SamplesSSM058
Known Genes
MethodSequencing
AnalysisBreakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads
PlatformIllumina HiSeq 2000
Comments
ReferenceWong_et_al_2012b
Pubmed ID23290073
Accession Number(s)essv6753927
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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