A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637828



Internal ID7024616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:8272667..8279110hg38UCSC Ensembl
Innerchr16:8272670..8279107hg38UCSC Ensembl
Outerchr16:8272664..8279113hg38UCSC Ensembl
chr16:8322669..8329112hg19UCSC Ensembl
Innerchr16:8322672..8329109hg19UCSC Ensembl
Outerchr16:8322666..8329115hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg386444
hg196444
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15368281, essv15368280
SamplesHG02494, HG03012
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637828
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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