A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576568



Internal ID16017291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:22760609..22882492hg38UCSC Ensembl
Innerchr18:20340572..20462455hg19UCSC Ensembl
Innerchr18:18594570..18716453hg18UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38121884
hg19121884
hg18121884
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv878494
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576568
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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