A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576829



Internal ID16364238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:48508798..48509957hg38UCSC Ensembl
Innerchr18:46035169..46036328hg19UCSC Ensembl
Innerchr18:44289167..44290326hg18UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg381160
hg191160
hg181160
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5917n54
Supporting Variantsnssv882722
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576829
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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