A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14085848



Internal ID21283174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:30952256..30964365hg38UCSC Ensembl
Innerchr8:30809772..30821881hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3812110
hg1912110
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110620
Supporting Variants
Samplessample34
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14085848
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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