A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv877291



Internal ID15824561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:394946..712037hg38UCSC Ensembl
Innerchr18:394946..712037hg19UCSC Ensembl
Innerchr18:384946..702037hg18UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg38317092
hg19317092
hg18317092
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576239
Supporting Variants
Samples
Known GenesC18orf56, CETN1, CLUL1, COLEC12, ENOSF1, TYMS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv877291
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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