A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060063



Internal ID19149282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:70497342..70557061hg38UCSC Ensembl
Innerchr18:68164578..68224297hg19UCSC Ensembl
Innerchr18:66315558..66375277hg18UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg3859720
hg1959720
hg1859720
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3562961
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)nsv1060063
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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