A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032066



Internal ID19121288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:139311333..139441597hg38UCSC Ensembl
Innerchr8:140323577..140453840hg19UCSC Ensembl
Innerchr8:140392759..140523022hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38130265
hg19130264
hg18130264
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7329n100
Supporting Variantsnssv3690068, nssv3690067
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)nsv1032066
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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