A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv882505



Internal ID16176461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:43392927..43533836hg38UCSC Ensembl
Innerchr18:40972892..41113801hg19UCSC Ensembl
Innerchr18:39226890..39367799hg18UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg38140910
hg19140910
hg18140910
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576770
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)nssv882505
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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