A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577481



Internal ID16364890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:69085217..69145197hg38UCSC Ensembl
Innerchr18:66752454..66812434hg19UCSC Ensembl
Innerchr18:64903434..64963414hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg3859981
hg1959981
hg1859981
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6036n54
Supporting Variantsnssv886853
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577481
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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