A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15436928



Internal ID5298715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:26083063..26103021hg38UCSC Ensembl
chr16:26094384..26114342hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3819959
hg1919959
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3638291
Supporting Variants
SamplesNA18749
Known GenesHS3ST4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15436928
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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