A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6916082



Internal ID9680365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:2539066..2540075hg38UCSC Ensembl
Outerchr12:2648232..2649241hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg381010
hg191010
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2745413
Supporting Variants
SamplesSSM016
Known GenesCACNA1C
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)essv6916082
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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