A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579425



Internal ID16366834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:36152793..36194851hg38UCSC Ensembl
Innerchr19:36643695..36685753hg19UCSC Ensembl
Innerchr19:41335535..41377593hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3842059
hg1942059
hg1842059
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv898985
Samples
Known GenesCOX7A1, ZNF565
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579425
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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