A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578151



Internal ID16365560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:567286..571320hg38UCSC Ensembl
Innerchr19:567286..571320hg19UCSC Ensembl
Innerchr19:518286..522320hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg384035
hg194035
hg184035
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv891221
Samples
Known GenesBSG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578151
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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