A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6691669



Internal ID9758166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:113299883..113300293hg38UCSC Ensembl
Outerchr12:113737688..113738098hg19UCSC Ensembl
Cytoband12q24.13
Allele length
AssemblyAllele length
hg38411
hg19411
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2746379
Supporting Variants
SamplesSSM036
Known GenesSLC8B1
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)essv6691669
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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