A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578159



Internal ID16365568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:581815..582693hg38UCSC Ensembl
Innerchr19:581815..582693hg19UCSC Ensembl
Innerchr19:532815..533693hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38879
hg19879
hg18879
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv891229
Samples
Known GenesBSG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578159
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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