A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv900960



Internal ID15848230
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 StatusS
Merged Variantsnsv580001
Supporting Variants
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)nssv900960
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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