A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063789



Internal ID19153008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:44608123..44650207hg38UCSC Ensembl
Innerchr18:42188088..42230172hg19UCSC Ensembl
Innerchr18:40442086..40484170hg18UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3842085
hg1942085
hg1842085
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3726071
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)nsv1063789
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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