A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv817854



Internal ID15765124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:98576454..98577494hg38UCSC Ensembl
Innerchr13:99228708..99229748hg19UCSC Ensembl
Innerchr13:98026709..98027749hg18UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg381041
hg191041
hg181041
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv562894
Supporting Variants
Samples
Known GenesSTK24
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv817854
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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