A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012160



Internal ID18754696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:162464378..162822690hg38UCSC Ensembl
Innerchr3:162182166..162540478hg19UCSC Ensembl
Innerchr3:163664860..164023172hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38358313
hg19358313
hg18358313
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3607952
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)nsv1012160
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