A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3691460



Internal ID18989741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:116618444..116640209hg38UCSC Ensembl
Innerchr8:117630683..117652448hg19UCSC Ensembl
Innerchr8:117699864..117721629hg18UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3821766
hg1921766
hg1821766
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1020480
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3691460
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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