A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3725180



Internal ID18676775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:575087..863351hg38UCSC Ensembl
Innerchr18:575087..863352hg19UCSC Ensembl
Innerchr18:565087..853352hg18UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg38288265
hg19288266
hg18288266
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1060188
Supporting Variants
Samples
Known GenesC18orf56, CETN1, CLUL1, ENOSF1, TYMS, YES1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3725180
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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