A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562891



Internal ID16003614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:98576401..98577494hg38UCSC Ensembl
Innerchr13:99228655..99229748hg19UCSC Ensembl
Innerchr13:98026656..98027749hg18UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg381094
hg191094
hg181094
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3347n54
Supporting Variantsnssv817847, nssv817846
Samples
Known GenesSTK24
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562891
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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