A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059909



Internal ID19149128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:43664868..43682424hg38UCSC Ensembl
Innerchr18:41244833..41262389hg19UCSC Ensembl
Innerchr18:39498831..39516387hg18UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3817557
hg1917557
hg1817557
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3565366
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)nsv1059909
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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