A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638658



Internal ID7025443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:53714789..53732556hg38UCSC Ensembl
Innerchr16:53714812..53732533hg38UCSC Ensembl
Outerchr16:53714766..53732579hg38UCSC Ensembl
chr16:53748701..53766468hg19UCSC Ensembl
Innerchr16:53748724..53766445hg19UCSC Ensembl
Outerchr16:53748678..53766491hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3817768
hg1917768
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15478920
SamplesHG00610
Known GenesFTO
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638658
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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