A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676990



Internal ID9943095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:74581717..74598293hg38UCSC Ensembl
Outerchr16:74581680..74598343hg38UCSC Ensembl
Innerchr16:74615615..74632191hg19UCSC Ensembl
Outerchr16:74615578..74632241hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3816664
hg1916664
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5636441
SamplesNA18530
Known GenesGLG1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2676990
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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