A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6883134



Internal ID9931616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:25415702..25559948hg38UCSC Ensembl
Outerchr22:25811669..25955915hg19UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg38144247
hg19144247
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2724087
Supporting Variants
SamplesSSM094
Known GenesCRYBB2P1, MIR6817
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)essv6883134
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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