A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3681578



Internal ID18979859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:8078321..8237241hg38UCSC Ensembl
Innerchr8:7935843..8094763hg19UCSC Ensembl
Innerchr8:7973253..8132173hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38158921
hg19158921
hg18158921
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1032822
Supporting Variants
Samples
Known GenesFAM86B3P, MIR548I3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3681578
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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