A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15569815



Internal ID5571631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89419179..89428256hg38UCSC Ensembl
Innerchr16:89419217..89428218hg38UCSC Ensembl
Outerchr16:89419141..89428294hg38UCSC Ensembl
chr16:89485587..89494664hg19UCSC Ensembl
Innerchr16:89485625..89494626hg19UCSC Ensembl
Outerchr16:89485549..89494702hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg389078
hg199078
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3639577
Supporting Variants
SamplesHG00335
Known GenesANKRD11
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15569815
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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