A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058723



Internal ID19147942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:76699084..76759346hg38UCSC Ensembl
Innerchr18:74411040..74471302hg19UCSC Ensembl
Innerchr18:72540028..72600290hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3860263
hg1960263
hg1860263
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3405n100
Supporting Variantsnssv3723235, nssv3563037
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)nsv1058723
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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