A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579330



Internal ID16366739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:33621607..33622257hg38UCSC Ensembl
Innerchr19:34112513..34113163hg19UCSC Ensembl
Innerchr19:38804353..38805003hg18UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38651
hg19651
hg18651
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6405n54
Supporting Variantsnssv898505, nssv898506, nssv898503, nssv898502, nssv898501, nssv898504
Samples
Known GenesCHST8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579330
Frequency
Sample Size17421
Observed Gain3
Observed Loss3
Observed Complex0
Frequencyn/a


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