A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579393



Internal ID16020116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35268346..35269961hg38UCSC Ensembl
Innerchr19:35759249..35760864hg19UCSC Ensembl
Innerchr19:40451089..40452704hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg381616
hg191616
hg181616
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6417n54
Supporting Variantsnssv898774
Samples
Known GenesUSF2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579393
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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