A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008526



Internal ID18751057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4080422..4189324hg38UCSC Ensembl
Innerchr3:4122106..4231008hg19UCSC Ensembl
Innerchr3:4097106..4206008hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38108903
hg19108903
hg18108903
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4650n100
Supporting Variantsnssv3590459
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1008526
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer