A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060747



Internal ID19149966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:53976012..53995477hg38UCSC Ensembl
Innerchr16:54009924..54029389hg19UCSC Ensembl
Innerchr16:52567425..52586890hg18UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3819466
hg1919466
hg1819466
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559267
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)nsv1060747
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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