A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638291



Internal ID7025077
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15436927, essv15436928
SamplesHG01031, NA18749
Known GenesHS3ST4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638291
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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