A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6862483



Internal ID10257953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:124945033..124945944hg38UCSC Ensembl
Outerchr12:125429579..125430490hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg38912
hg19912
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2746551
Supporting Variants
SamplesSSM088
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)essv6862483
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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