A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3674906



Internal ID18626501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:96386..460640hg38UCSC Ensembl
Innerchr8:46386..410640hg19UCSC Ensembl
Innerchr8:36386..400640hg18UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg38364255
hg19364255
hg18364255
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1034957
Supporting Variants
Samples
Known GenesFAM87A, FBXO25, OR4F21, RPL23AP53, ZNF596
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3674906
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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