A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637985



Internal ID7024771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:13543537..13555832hg38UCSC Ensembl
chr16:13637394..13649689hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3812296
hg1912296
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15378561
SamplesHG01889
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637985
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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