A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv884852



Internal ID16178808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:57493400..57518698hg38UCSC Ensembl
Innerchr18:55160632..55185930hg19UCSC Ensembl
Innerchr18:53311630..53336928hg18UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg3825299
hg1925299
hg1825299
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv577030
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv884852
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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