A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067376



Internal ID19156595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:27257073..27682965hg38UCSC Ensembl
Innerchr19:27747981..28173873hg19UCSC Ensembl
Innerchr19:32439821..32865713hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38425893
hg19425893
hg18425893
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3499n100
Supporting Variantsnssv3572035
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)nsv1067376
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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