A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576589



Internal ID16363998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:26991760..26992277hg38UCSC Ensembl
Innerchr18:24571724..24572241hg19UCSC Ensembl
Innerchr18:22825722..22826239hg18UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38518
hg19518
hg18518
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5876n54
Supporting Variantsnssv878865
Samples
Known GenesCHST9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576589
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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