A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042928



Internal ID18785459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:5114681..5298137hg38UCSC Ensembl
Innerchr16:5164682..5348138hg19UCSC Ensembl
Innerchr16:5104683..5288139hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38183457
hg19183457
hg18183457
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2696n100
Supporting Variantsnssv3718835
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)nsv1042928
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