A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060949



Internal ID18803480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:53713622..53761724hg38UCSC Ensembl
Innerchr16:53747534..53795636hg19UCSC Ensembl
Innerchr16:52305035..52353137hg18UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3848103
hg1948103
hg1848103
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559266
Samples
Known GenesFTO
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060949
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