A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3690065



Internal ID18988346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:139306124..139441231hg38UCSC Ensembl
Innerchr8:140318368..140453474hg19UCSC Ensembl
Innerchr8:140387550..140522656hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38135108
hg19135107
hg18135107
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1034929
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)nssv3690065
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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