A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579397



Internal ID16020120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35268699..35269902hg38UCSC Ensembl
Innerchr19:35759602..35760805hg19UCSC Ensembl
Innerchr19:40451442..40452645hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg381204
hg191204
hg181204
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6418n54
Supporting Variantsnssv898779
Samples
Known GenesUSF2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579397
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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