A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv885016



Internal ID16178972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:65323304..65354749hg38UCSC Ensembl
Innerchr18:62990540..63021985hg19UCSC Ensembl
Innerchr18:61141520..61172965hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg3831446
hg1931446
hg1831446
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv577112
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)nssv885016
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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