A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2715123



Internal ID9949409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:89166502..89166750hg38UCSC Ensembl
Outerchr16:89232910..89233158hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38249
hg19249
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6843086, essv6725100, essv6772692, essv6717410
SamplesSSM065, SSM084, SSM043, SSM045
Known GenesLOC400558
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)esv2715123
Frequency
Sample Size96
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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