A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170026



Internal ID21314087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:160845337..160885289hg38UCSC Ensembl
Outerchr4:160842284..160887019hg38UCSC Ensembl
Innerchr4:161766489..161806441hg19UCSC Ensembl
Outerchr4:161763436..161808171hg19UCSC Ensembl
Innerchr4:161985939..162025891hg18UCSC Ensembl
Outerchr4:161982886..162027621hg18UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3844736
hg1944736
hg1844736
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14246227
SamplesNGO_32
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170026
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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