A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3687372



Internal ID18985653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:45935900..46151810hg38UCSC Ensembl
Innerchr8:46847522..47063432hg19UCSC Ensembl
Innerchr8:46966687..47182597hg18UCSC Ensembl
Cytoband8q11.1
Allele length
AssemblyAllele length
hg38215911
hg19215911
hg18215911
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028273
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)nssv3687372
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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