A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6781569



Internal ID10186302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:185794261..185794494hg38UCSC Ensembl
Outerchr3:185512049..185512282hg19UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg38234
hg19234
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2726326, esv2726327
Supporting Variants
SamplesSSM068
Known GenesIGF2BP2
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)essv6781569
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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