A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578615



Internal ID16019338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:11322813..11344363hg38UCSC Ensembl
Innerchr19:11433489..11455039hg19UCSC Ensembl
Innerchr19:11294489..11316039hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3821551
hg1921551
hg1821551
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv893551
Samples
Known GenesRAB3D, TMEM205, TSPAN16
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578615
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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