A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578299



Internal ID16365708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1566455..1567288hg38UCSC Ensembl
Innerchr19:1566454..1567287hg19UCSC Ensembl
Innerchr19:1517454..1518287hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38834
hg19834
hg18834
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv891809, nssv891810
Samples
Known GenesMEX3D
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578299
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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