A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066584



Internal ID19155803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:27859862..27928435hg38UCSC Ensembl
Innerchr18:25439826..25508399hg19UCSC Ensembl
Innerchr18:23693824..23762397hg18UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3868574
hg1968574
hg1868574
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564146
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)nsv1066584
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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