A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2714809



Internal ID9949094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:83723865..83724686hg38UCSC Ensembl
Outerchr16:83757470..83758291hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg38822
hg19822
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6882772, essv6913191, essv6936800, essv6665624, essv6916686
SamplesSSM016, SSM094, SSM029, SSM021, SSM015
Known GenesCDH13
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)esv2714809
Frequency
Sample Size96
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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