A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562886



Internal ID16003609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:98576349..98577256hg38UCSC Ensembl
Innerchr13:99228603..99229510hg19UCSC Ensembl
Innerchr13:98026604..98027511hg18UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg38908
hg19908
hg18908
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3349n54
Supporting Variantsnssv817806, nssv817803, nssv817807, nssv817802, nssv817804, nssv817805, nssv817808
Samples
Known GenesSTK24
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562886
Frequency
Sample Size17421
Observed Gain3
Observed Loss4
Observed Complex0
Frequencyn/a


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