A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639514



Internal ID7026294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87385280..87387643hg38UCSC Ensembl
Innerchr16:87385326..87387597hg38UCSC Ensembl
Outerchr16:87385234..87387689hg38UCSC Ensembl
chr16:87418886..87421249hg19UCSC Ensembl
Innerchr16:87418932..87421203hg19UCSC Ensembl
Outerchr16:87418840..87421295hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg382364
hg192364
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15555135, essv15555136
SamplesHG01250, HG01137
Known GenesFBXO31
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639514
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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