A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3675290



Internal ID18973571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:2492800..2725657hg38UCSC Ensembl
Innerchr8:2349916..2583198hg19UCSC Ensembl
Innerchr8:2337323..2570605hg18UCSC Ensembl
Cytoband8p23.2
Allele length
AssemblyAllele length
hg38232858
hg19233283
hg18233283
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1016370
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)nssv3675290
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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