A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169698



Internal ID21313509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:88395967..88470472hg38UCSC Ensembl
Outerchr8:88388491..88481173hg38UCSC Ensembl
Innerchr8:89408196..89482701hg19UCSC Ensembl
Outerchr8:89400720..89493402hg19UCSC Ensembl
Innerchr8:89477312..89551817hg18UCSC Ensembl
Outerchr8:89469836..89562518hg18UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3892683
hg1992683
hg1892683
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14247068
SamplesNGO_32
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169698
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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