A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv877418



Internal ID15824688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:2278802..2566394hg38UCSC Ensembl
Innerchr18:2278801..2566393hg19UCSC Ensembl
Innerchr18:2268801..2556393hg18UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg38287593
hg19287593
hg18287593
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576310
Supporting Variants
Samples
Known GenesMETTL4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv877418
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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