A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv963012



Internal ID15910282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:48464823..48478412hg38UCSC Ensembl
Innerchr3:48506222..48519821hg19UCSC Ensembl
Innerchr3:48481226..48494825hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3813590
hg1913600
hg1813600
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590245
Supporting Variants
Samples
Known GenesATRIP, SHISA5, TREX1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv963012
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