A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579337



Internal ID16366746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:33621709..33622360hg38UCSC Ensembl
Innerchr19:34112615..34113266hg19UCSC Ensembl
Innerchr19:38804455..38805106hg18UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38652
hg19652
hg18652
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6406n54
Supporting Variantsnssv898549, nssv898551, nssv898546, nssv898554, nssv898552, nssv898548, nssv898553, nssv898550, nssv898547
Samples
Known GenesCHST8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579337
Frequency
Sample Size17421
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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