A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14083331



Internal ID21292304
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 StatusS
Merged Variantsnsv3112465
Supporting Variants
Samplessample87
Known GenesHDAC9
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14083331
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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