A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065724



Internal ID19154943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:27257073..27509930hg38UCSC Ensembl
Innerchr19:27747981..28000838hg19UCSC Ensembl
Innerchr19:32439821..32692678hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38252858
hg19252858
hg18252858
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3498n100
Supporting Variantsnssv3570859, nssv3570860, nssv3570858
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)nsv1065724
Frequency
Sample Size11257
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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