A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639564



Internal ID6679655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88956113..88958120hg38UCSC Ensembl
Innerchr16:88956132..88958102hg38UCSC Ensembl
Outerchr16:88956095..88958139hg38UCSC Ensembl
chr16:89022521..89024528hg19UCSC Ensembl
Innerchr16:89022540..89024510hg19UCSC Ensembl
Outerchr16:89022503..89024547hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg382008
hg192008
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15567781
SamplesNA18611
Known GenesCBFA2T3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639564
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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