A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064305



Internal ID19153524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:27257073..27374984hg38UCSC Ensembl
Innerchr19:27747981..27865892hg19UCSC Ensembl
Innerchr19:32439821..32557732hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38117912
hg19117912
hg18117912
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3494n100
Supporting Variantsnssv3570797
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)nsv1064305
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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