A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065451



Internal ID19154670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:22452760..22486002hg38UCSC Ensembl
Innerchr18:20032723..20065965hg19UCSC Ensembl
Innerchr18:18286721..18319963hg18UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3833243
hg1933243
hg1833243
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564131
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065451
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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