A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6906381



Internal ID9674109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:33556244..33556534hg38UCSC Ensembl
Outerchr2:33781311..33781601hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38291
hg19291
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2719890
Supporting Variants
SamplesSSM014
Known GenesRASGRP3
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)essv6906381
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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