A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041660



Internal ID18784191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:5307559..5327717hg38UCSC Ensembl
Innerchr16:5357560..5377718hg19UCSC Ensembl
Innerchr16:5297561..5317719hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3820159
hg1920159
hg1820159
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2698n100
Supporting Variantsnssv3556997
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)nsv1041660
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