A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv898778



Internal ID15846048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35268614..35272793hg38UCSC Ensembl
Innerchr19:35759517..35763696hg19UCSC Ensembl
Innerchr19:40451357..40455536hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg384180
hg194180
hg184180
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579396
Supporting Variants
Samples
Known GenesUSF2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv898778
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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