A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6842665



Internal ID10241880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:112199215..112199532hg38UCSC Ensembl
Outerchr13:112853529..112853846hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2748133
Supporting Variants
SamplesSSM084
Known GenesLINC01070
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)essv6842665
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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