A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6667722



Internal ID9645225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:25257977..25506551hg38UCSC Ensembl
Outerchr22:25653944..25902518hg19UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg38248575
hg19248575
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2724085, esv2724081
Supporting Variants
SamplesSSM004
Known GenesCRYBB2P1, IGLL3P, LRP5L, 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)essv6667722
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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