A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024081



Internal ID19113298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:139529474..139579986hg38UCSC Ensembl
Innerchr8:140541717..140592229hg19UCSC Ensembl
Innerchr8:140610899..140661411hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3850513
hg1950513
hg1850513
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3690070
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)nsv1024081
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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