A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv555e214



Internal ID18980730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89428478..89441505hg38UCSC Ensembl
chr16:89494886..89507913hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3813028
hg1913028
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3639578, esv3639580
SamplesHG01798
Known GenesANKRD11
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv555e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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