A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv875837



Internal ID16169793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:66102427..66208473hg38UCSC Ensembl
Innerchr17:64098545..64204591hg19UCSC Ensembl
Innerchr17:61529007..61635053hg18UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg38106047
hg19106047
hg18106047
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv575891
Supporting Variants
Samples
Known GenesCEP112
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv875837
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