A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579468



Internal ID16020191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:37486707..37802847hg38UCSC Ensembl
Innerchr19:37977609..38293487hg19UCSC Ensembl
Innerchr19:42669449..42985327hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38316141
hg19315879
hg18315879
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv899163
Samples
Known GenesZFP30, ZNF540, ZNF571, ZNF571-AS1, ZNF573, ZNF607, ZNF781, ZNF793
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579468
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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