A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639578



Internal ID6679669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89428478..89441377hg38UCSC Ensembl
chr16:89494886..89507785hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3812900
hg1912900
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv555e214
Supporting Variantsessv15569816
SamplesHG01798
Known GenesANKRD11
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639578
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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