A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638657



Internal ID6678754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:53713016..53717342hg38UCSC Ensembl
Innerchr16:53713024..53717334hg38UCSC Ensembl
Outerchr16:53713008..53717350hg38UCSC Ensembl
chr16:53746928..53751254hg19UCSC Ensembl
Innerchr16:53746936..53751246hg19UCSC Ensembl
Outerchr16:53746920..53751262hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg384327
hg194327
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15478919
SamplesHG02943
Known GenesFTO
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638657
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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