A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063197



Internal ID19152416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:15326730..15401752hg38UCSC Ensembl
Innerchr18:15326729..15401751hg19UCSC Ensembl
Innerchr18:15316729..15391751hg18UCSC Ensembl
Cytoband18p11.1
Allele length
AssemblyAllele length
hg3875023
hg1975023
hg1875023
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564125
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)nsv1063197
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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