A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3690066



Internal ID18988347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:139311333..139403743hg38UCSC Ensembl
Innerchr8:140323577..140415986hg19UCSC Ensembl
Innerchr8:140392759..140485168hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3892411
hg1992410
hg1892410
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1016626
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)nssv3690066
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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