A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562881



Internal ID16003604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:98576248..98577256hg38UCSC Ensembl
Innerchr13:99228502..99229510hg19UCSC Ensembl
Innerchr13:98026503..98027511hg18UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg381009
hg191009
hg181009
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3346n54
Supporting Variantsnssv817793
Samples
Known GenesSTK24
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562881
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer