A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637889



Internal ID7024677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10186736..10267702hg38UCSC Ensembl
Innerchr16:10187236..10267202hg38UCSC Ensembl
Outerchr16:10185736..10268702hg38UCSC Ensembl
chr16:10280593..10361559hg19UCSC Ensembl
Innerchr16:10281093..10361059hg19UCSC Ensembl
Outerchr16:10279593..10362559hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3880967
hg1980967
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15373003
SamplesNA18740
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637889
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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