A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149965



Internal ID15853981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43001832..43191688hg38UCSC Ensembl
Innerchr19:43505984..43695840hg19UCSC Ensembl
Innerchr19:48197824..48387680hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38189857
hg19189857
hg18189857
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579772
Supporting Variants
Samples1780854499_A
Known GenesPSG11, PSG2, PSG5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149965
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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