A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv885018



Internal ID16178974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:65494948..65542167hg38UCSC Ensembl
Innerchr18:63162184..63209403hg19UCSC Ensembl
Innerchr18:61313164..61360383hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg3847220
hg1947220
hg1847220
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv577114
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv885018
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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