A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169359



Internal ID21313842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:27679132..27776438hg38UCSC Ensembl
Outerchr14:27669078..27784005hg38UCSC Ensembl
Innerchr14:28148338..28245644hg19UCSC Ensembl
Outerchr14:28138284..28253211hg19UCSC Ensembl
Innerchr14:27218178..27315484hg18UCSC Ensembl
Outerchr14:27208124..27323051hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38114928
hg19114928
hg18114928
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14250832
SamplesNGO_18
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169359
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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