A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578363



Internal ID16365772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1950671..1951333hg38UCSC Ensembl
Innerchr19:1950670..1951332hg19UCSC Ensembl
Innerchr19:1901670..1902332hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38663
hg19663
hg18663
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv892041
Samples
Known GenesCSNK1G2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578363
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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