A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6920259



Internal ID9683824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:117465581..117465965hg38UCSC Ensembl
Outerchr12:117903386..117903770hg19UCSC Ensembl
Cytoband12q24.22
Allele length
AssemblyAllele length
hg38385
hg19385
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2746440
Supporting Variants
SamplesSSM017
Known GenesKSR2
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)essv6920259
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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