A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059139



Internal ID19148358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:66701778..66981041hg38UCSC Ensembl
Innerchr18:64369015..64648278hg19UCSC Ensembl
Innerchr18:62519995..62799258hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38279264
hg19279264
hg18279264
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3723119
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)nsv1059139
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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