A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579704



Internal ID16367113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42866627..42937899hg38UCSC Ensembl
Innerchr19:43370779..43442051hg19UCSC Ensembl
Innerchr19:48062619..48133891hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3871273
hg1971273
hg1871273
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv899715
Samples
Known GenesPSG1, PSG6, PSG7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579704
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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