A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639575



Internal ID6679666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89351809..89353290hg38UCSC Ensembl
Innerchr16:89351830..89353269hg38UCSC Ensembl
Outerchr16:89351788..89353311hg38UCSC Ensembl
chr16:89418217..89419698hg19UCSC Ensembl
Innerchr16:89418238..89419677hg19UCSC Ensembl
Outerchr16:89418196..89419719hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg381482
hg191482
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15569813, essv15569812
SamplesNA19904, HG03391
Known GenesANKRD11
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639575
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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