A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6749982



Internal ID10157358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:66341420..66341789hg38UCSC Ensembl
Outerchr15:66633758..66634127hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38370
hg19370
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2749790
Supporting Variants
SamplesSSM056
Known GenesTIPIN
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)essv6749982
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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