A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1105802



Internal ID15958988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:7535252..7598872hg38UCSC Ensembl
Innerchr8:7392774..7456394hg19UCSC Ensembl
Innerchr8:7380184..7443804hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3863621
hg1963621
hg1863621
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv610093
Supporting Variants
Samples
Known GenesFAM90A7P, PRR23D1, PRR23D2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1105802
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