A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv877289



Internal ID15824559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:351004..1913315hg38UCSC Ensembl
Innerchr18:351004..1913316hg19UCSC Ensembl
Innerchr18:341004..1903316hg18UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg381562312
hg191562313
hg181562313
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576237
Supporting Variants
Samples
Known GenesADCYAP1, C18orf56, CETN1, CLUL1, COLEC12, ENOSF1, LINC00470, TYMS, YES1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv877289
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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