A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6945394



Internal ID10049774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:36662297..36662656hg38UCSC Ensembl
Outerchr15:36954498..36954857hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38360
hg19360
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2749571
Supporting Variants
SamplesSSM023
Known GenesC15orf41
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)essv6945394
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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