A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv898985



Internal ID16192941
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 StatusS
Merged Variantsnsv579425
Supporting Variants
Samples
Known GenesCOX7A1, ZNF565
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv898985
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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