A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579394



Internal ID16020117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35268346..35270070hg38UCSC Ensembl
Innerchr19:35759249..35760973hg19UCSC Ensembl
Innerchr19:40451089..40452813hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg381725
hg191725
hg181725
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6417n54
Supporting Variantsnssv898776, nssv898775
Samples
Known GenesUSF2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579394
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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