A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639569



Internal ID6679660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89124194..89131476hg38UCSC Ensembl
Innerchr16:89124694..89130976hg38UCSC Ensembl
Outerchr16:89123194..89132476hg38UCSC Ensembl
chr16:89190602..89197884hg19UCSC Ensembl
Innerchr16:89191102..89197384hg19UCSC Ensembl
Outerchr16:89189602..89198884hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg387283
hg197283
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15567788, essv15567790, essv15567789
SamplesHG01589, NA20795, NA20797
Known GenesACSF3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639569
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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