A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3675051



Internal ID18626646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:1588960..1652691hg38UCSC Ensembl
Innerchr8:1537126..1600857hg19UCSC Ensembl
Innerchr8:1524533..1588264hg18UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg3863732
hg1963732
hg1863732
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1018421
Supporting Variants
Samples
Known GenesDLGAP2, LOC100507435
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3675051
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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