A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6939114



Internal ID9699766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:136269611..136273067hg38UCSC Ensembl
Outerchr6:136590749..136594205hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg383457
hg193457
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2732749
Supporting Variants
SamplesSSM022
Known GenesBCLAF1
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)essv6939114
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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