A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112465



Internal ID21295731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:18996617..19114448hg38UCSC Ensembl
Innerchr7:19036240..19154071hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38117832
hg19117832
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14083331
Samplessample87
Known GenesHDAC9
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112465
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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