A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv899813



Internal ID16193769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43079534..43174544hg38UCSC Ensembl
Innerchr19:43583686..43678696hg19UCSC Ensembl
Innerchr19:48275526..48370536hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3895011
hg1995011
hg1895011
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579783
Supporting Variants
Samples
Known GenesPSG2, PSG5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv899813
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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