A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3589598



Internal ID18887879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:35449219..35552716hg38UCSC Ensembl
Innerchr3:35490711..35594208hg19UCSC Ensembl
Innerchr3:35465715..35569212hg18UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38103498
hg19103498
hg18103498
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1009907
Supporting Variants
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)nssv3589598
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