A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6843089



Internal ID9895574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:89455036..89455271hg38UCSC Ensembl
Outerchr16:89521444..89521679hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38236
hg19236
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2715164, esv2715162
Supporting Variants
SamplesSSM084
Known GenesANKRD11
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)essv6843089
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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