A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576236



Internal ID16016959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:319176..794272hg38UCSC Ensembl
Innerchr18:319176..794273hg19UCSC Ensembl
Innerchr18:309176..784273hg18UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg38475097
hg19475098
hg18475098
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv877288
Samples
Known GenesC18orf56, CETN1, CLUL1, COLEC12, ENOSF1, TYMS, YES1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576236
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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