A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580001



Internal ID16367410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:51798407..52013985hg38UCSC Ensembl
Innerchr19:52301660..52517238hg19UCSC Ensembl
Innerchr19:56993472..57209050hg18UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg38215579
hg19215579
hg18215579
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv900960
Samples
Known GenesFPR3, HCCAT3, ZNF350, ZNF577, ZNF613, ZNF614, ZNF615, ZNF649
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580001
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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