A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3689703



Internal ID18987984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:89593216..89710352hg38UCSC Ensembl
Innerchr8:90605445..90722580hg19UCSC Ensembl
Innerchr8:90674561..90791702hg18UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38117137
hg19117136
hg18117142
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1017263
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)nssv3689703
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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