A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056628



Internal ID19145847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:27257073..27690007hg38UCSC Ensembl
Innerchr19:27747981..28180915hg19UCSC Ensembl
Innerchr19:32439821..32872755hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38432935
hg19432935
hg18432935
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3499n100
Supporting Variantsnssv3572036
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)nsv1056628
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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