A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3675899



Internal ID18627494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:15444894..15812092hg38UCSC Ensembl
Innerchr8:15302403..15669601hg19UCSC Ensembl
Innerchr8:15346774..15713972hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38367199
hg19367199
hg18367199
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1020054
Supporting Variants
Samples
Known GenesTUSC3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3675899
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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