A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6922614



Internal ID9685110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:68853100..69457137hg38UCSC Ensembl
Outerchr4:69718818..70322855hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38604038
hg19604038
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2727775
Supporting Variants
SamplesSSM018
Known GenesUGT2A3, UGT2B10, UGT2B11, UGT2B28, UGT2B7
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)essv6922614
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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