A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1124934



Internal ID15978120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:142681514..142684467hg38UCSC Ensembl
Innerchr8:143762932..143765885hg19UCSC Ensembl
Innerchr8:143759934..143762887hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg382954
hg192954
hg182954
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv612712
Supporting Variants
Samples
Known GenesPSCA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1124934
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