A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572619



Internal ID16360028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:53839191..53882596hg38UCSC Ensembl
Innerchr16:53873103..53916508hg19UCSC Ensembl
Innerchr16:52430604..52474009hg18UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3843406
hg1943406
hg1843406
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv857463
Samples
Known GenesFTO
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572619
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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