A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063458



Internal ID19152677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:24174779..24413936hg38UCSC Ensembl
Innerchr19:24357581..24596738hg19UCSC Ensembl
Innerchr19:24149421..24388578hg18UCSC Ensembl
Cytoband19p11
Allele length
AssemblyAllele length
hg38239158
hg19239158
hg18239158
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3483n100
Supporting Variantsnssv3570660
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)nsv1063458
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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