A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv877293



Internal ID15824563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:563815..1831298hg38UCSC Ensembl
Innerchr18:563815..1831299hg19UCSC Ensembl
Innerchr18:553815..1821299hg18UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg381267484
hg191267485
hg181267485
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576241
Supporting Variants
Samples
Known GenesADCYAP1, C18orf56, CETN1, CLUL1, ENOSF1, LINC00470, TYMS, YES1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv877293
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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