A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6845941



Internal ID9898143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:11267201..11393845hg38UCSC Ensembl
Outerchr12:11420134..11546779hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg38126645
hg19126646
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2745556
Supporting Variants
SamplesSSM085
Known GenesPRB1, PRB2, PRB3, PRB4
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)essv6845941
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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