A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058446



Internal ID19147665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:78119835..78291087hg38UCSC Ensembl
Innerchr18:75879835..76051087hg19UCSC Ensembl
Innerchr18:73980823..74152075hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38171253
hg19171253
hg18171253
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3563045
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)nsv1058446
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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