A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013626



Internal ID18756158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:46761415..46807677hg38UCSC Ensembl
Innerchr3:46802905..46849167hg19UCSC Ensembl
Innerchr3:46777909..46824171hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3846263
hg1946263
hg1846263
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4736n100
Supporting Variantsnssv3593812
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)nsv1013626
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