A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062660



Internal ID18805191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:57848645..57945049hg38UCSC Ensembl
Innerchr16:57882549..57978953hg19UCSC Ensembl
Innerchr16:56440050..56536454hg18UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg3896405
hg1996405
hg1896405
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3722715
Samples
Known GenesCNGB1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1062660
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