A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv891586



Internal ID15838856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1095062..1124032hg38UCSC Ensembl
Innerchr19:1095061..1124031hg19UCSC Ensembl
Innerchr19:1046061..1075031hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3828971
hg1928971
hg1828971
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578215
Supporting Variants
Samples
Known GenesGPX4, POLR2E, SBNO2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv891586
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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