A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6718443



Internal ID10132928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:27101268..27101635hg38UCSC Ensembl
Outerchr2:27324136..27324503hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38368
hg19368
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2719833
Supporting Variants
SamplesSSM044
Known GenesCGREF1
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)essv6718443
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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