A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3564080



Internal ID18515675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:5012384..5236844hg38UCSC Ensembl
Innerchr18:5012383..5236843hg19UCSC Ensembl
Innerchr18:5002383..5226843hg18UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg38224461
hg19224461
hg18224461
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1065883
Supporting Variants
Samples
Known GenesC18orf42, LINC00526
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3564080
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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