A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6920709



Internal ID9684228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:3054007..3073675hg38UCSC Ensembl
Outerchr16:3104008..3123676hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3819669
hg1919669
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2750390
Supporting Variants
SamplesSSM017
Known GenesIL32, MMP25
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)essv6920709
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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