A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579332



Internal ID16366741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:33621607..33622360hg38UCSC Ensembl
Innerchr19:34112513..34113266hg19UCSC Ensembl
Innerchr19:38804353..38805106hg18UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38754
hg19754
hg18754
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6405n54
Supporting Variantsnssv898536, nssv898521, nssv898538, nssv898513, nssv898527, nssv898524, nssv898519, nssv898534, nssv898520, nssv898533, nssv898530, nssv898516, nssv898523, nssv898537, nssv898514, nssv898522, nssv898515, nssv898532, nssv898529, nssv898526, nssv898535, nssv898528, nssv898539, nssv898517, nssv898531, nssv898525, nssv898518
Samples
Known GenesCHST8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579332
Frequency
Sample Size17421
Observed Gain26
Observed Loss1
Observed Complex0
Frequencyn/a


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