A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv898497



Internal ID15845767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:33620377..33622206hg38UCSC Ensembl
Innerchr19:34111283..34113112hg19UCSC Ensembl
Innerchr19:38803123..38804952hg18UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg381830
hg191830
hg181830
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579327
Supporting Variants
Samples
Known GenesCHST8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv898497
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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