A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149963



Internal ID15875527
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
SamplesHGDP00696
Known GenesPSG11, PSG2, PSG5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149963
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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