A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv963093



Internal ID16257049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:52502292..52523424hg38UCSC Ensembl
Innerchr3:52536308..52557440hg19UCSC Ensembl
Innerchr3:52511348..52532480hg18UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg3821133
hg1921133
hg1821133
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590306
Supporting Variants
Samples
Known GenesSTAB1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv963093
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