A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv886252



Internal ID16180208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:66948348..67054881hg38UCSC Ensembl
Innerchr18:64615585..64722118hg19UCSC Ensembl
Innerchr18:62766565..62873098hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38106534
hg19106534
hg18106534
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv577286
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)nssv886252
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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