A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576892



Internal ID16017615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:50746815..50899947hg38UCSC Ensembl
Innerchr18:48273185..48426317hg19UCSC Ensembl
Innerchr18:46527183..46680315hg18UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg38153133
hg19153133
hg18153133
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv883092
Samples
Known GenesME2, MRO
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576892
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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