A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15569879



Internal ID5571695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89829646..89831997hg38UCSC Ensembl
Innerchr16:89829646..89831997hg38UCSC Ensembl
Outerchr16:89829303..89832327hg38UCSC Ensembl
chr16:89896054..89898405hg19UCSC Ensembl
Innerchr16:89896054..89898405hg19UCSC Ensembl
Outerchr16:89895711..89898735hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg382352
hg192352
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3639600
Supporting Variants
SamplesHG00127
Known GenesSPIRE2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15569879
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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