A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997589



Internal ID18810439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:177817742..177839387hg38UCSC Ensembl
Innerchr3:177535530..177557175hg19UCSC Ensembl
Innerchr3:179018224..179039869hg18UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3821646
hg1921646
hg1821646
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3614982, nssv3614983
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)nsv997589
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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