A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579329



Internal ID16366738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:33621607..33622206hg38UCSC Ensembl
Innerchr19:34112513..34113112hg19UCSC Ensembl
Innerchr19:38804353..38804952hg18UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38600
hg19600
hg18600
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv898500
Samples
Known GenesCHST8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579329
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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