A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6852972



Internal ID10251157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:44619358..44619711hg38UCSC Ensembl
Outerchr22:45015238..45015591hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg38354
hg19354
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2724355, esv2724356
Supporting Variants
SamplesSSM086
Known GenesLINC00229
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)essv6852972
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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