A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578619



Internal ID16019342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:11819824..12247907hg38UCSC Ensembl
Innerchr19:11930639..12358722hg19UCSC Ensembl
Innerchr19:11791639..12219722hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38428084
hg19428084
hg18428084
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv893554
Samples
Known GenesLOC100289333, ZNF136, ZNF20, ZNF433, ZNF439, ZNF440, ZNF625, ZNF625-ZNF20, ZNF69, ZNF700, ZNF763, ZNF788, ZNF844, ZNF878
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578619
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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