A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv976390



Internal ID16270346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:149235238..149251541hg38UCSC Ensembl
Innerchr3:148953025..148969328hg19UCSC Ensembl
Innerchr3:150435715..150452018hg18UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3816304
hg1916304
hg1816304
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv591978
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv976390
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