A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14100242



Internal ID21286104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:221221231..221236380hg38UCSC Ensembl
Innerchr1:221394573..221409722hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg3815150
hg1915150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114254
Supporting Variants
Samplessample383
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14100242
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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