A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065484



Internal ID19154703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:48459801..48485310hg38UCSC Ensembl
Innerchr18:45986172..46011681hg19UCSC Ensembl
Innerchr18:44240170..44265679hg18UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg3825510
hg1925510
hg1825510
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3565437
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)nsv1065484
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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