A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3589713



Internal ID18887994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:41842047..41947832hg38UCSC Ensembl
Innerchr3:41883539..41989324hg19UCSC Ensembl
Innerchr3:41858543..41964328hg18UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38105786
hg19105786
hg18105786
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1004339
Supporting Variants
Samples
Known GenesULK4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3589713
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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