A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638337



Internal ID6678435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:28566843..28596255hg38UCSC Ensembl
chr16:28578164..28607576hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3829413
hg1929413
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15440053, essv15440055, essv15440054
SamplesHG03742, HG03854, HG03594
Known GenesCCDC101, SULT1A2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638337
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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