A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6825695



Internal ID10226608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:171502940..171503172hg38UCSC Ensembl
Outerchr3:171220729..171220961hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg38233
hg19233
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2726202, esv2726201
Supporting Variants
SamplesSSM080
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)essv6825695
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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