A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638980



Internal ID7025764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:71831043..71836089hg38UCSC Ensembl
Innerchr16:71831543..71835589hg38UCSC Ensembl
Outerchr16:71830043..71837089hg38UCSC Ensembl
chr16:71864946..71869992hg19UCSC Ensembl
Innerchr16:71865446..71869492hg19UCSC Ensembl
Outerchr16:71863946..71870992hg19UCSC Ensembl
Cytoband16q22.2
Allele length
AssemblyAllele length
hg385047
hg195047
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15514813, essv15514814, essv15514812
SamplesHG01389, HG01357, HG01494
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638980
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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