A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058718



Internal ID19147937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:73393281..73451538hg38UCSC Ensembl
Innerchr18:71060516..71118773hg19UCSC Ensembl
Innerchr18:69211496..69269753hg18UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3858258
hg1958258
hg1858258
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3562979
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)nsv1058718
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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