A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576661



Internal ID16364070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:37721977..37726646hg38UCSC Ensembl
Innerchr18:35301940..35306609hg19UCSC Ensembl
Innerchr18:33555938..33560607hg18UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg384670
hg194670
hg184670
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv878968
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576661
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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