A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3675615



Internal ID18973896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:5932580..6189139hg38UCSC Ensembl
Innerchr8:5790102..6046660hg19UCSC Ensembl
Innerchr8:5777510..6034068hg18UCSC Ensembl
Cytoband8p23.2
Allele length
AssemblyAllele length
hg38256560
hg19256559
hg18256559
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1031618
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)nssv3675615
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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