A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043667



Internal ID18786198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:8757711..8773739hg38UCSC Ensembl
Innerchr16:8851568..8867596hg19UCSC Ensembl
Innerchr16:8759069..8775097hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3816029
hg1916029
hg1816029
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3557108
Samples
Known GenesABAT
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043667
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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