A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3687369



Internal ID18985650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:45935900..46043073hg38UCSC Ensembl
Innerchr8:46847522..46954695hg19UCSC Ensembl
Innerchr8:46966687..47073860hg18UCSC Ensembl
Cytoband8q11.1
Allele length
AssemblyAllele length
hg38107174
hg19107174
hg18107174
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1033056
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)nssv3687369
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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