A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579395



Internal ID16020118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35268614..35270070hg38UCSC Ensembl
Innerchr19:35759517..35760973hg19UCSC Ensembl
Innerchr19:40451357..40452813hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg381457
hg191457
hg181457
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6418n54
Supporting Variantsnssv898777
Samples
Known GenesUSF2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579395
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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