A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3723235



Internal ID19021516
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 StatusS
Merged Variantsnsv1058723
Supporting Variants
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)nssv3723235
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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