A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6827775



Internal ID10228480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:105496965..105497334hg38UCSC Ensembl
Outerchr12:105890743..105891112hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg38370
hg19370
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2746328, esv2746327
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)essv6827775
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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