A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6387641



Internal ID9002518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:53714819..53732537hg38UCSC Ensembl
Outerchr16:53714771..53732587hg38UCSC Ensembl
Innerchr16:53748731..53766449hg19UCSC Ensembl
Outerchr16:53748683..53766499hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3817817
hg1917817
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2671392
Supporting Variants
SamplesHG00610
Known GenesFTO
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6387641
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer