A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15569818



Internal ID5571634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89428666..89441505hg38UCSC Ensembl
Innerchr16:89428666..89441505hg38UCSC Ensembl
Outerchr16:89428329..89441844hg38UCSC Ensembl
chr16:89495074..89507913hg19UCSC Ensembl
Innerchr16:89495074..89507913hg19UCSC Ensembl
Outerchr16:89494737..89508252hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3812840
hg1912840
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3639580
Supporting Variants
SamplesHG01798
Known GenesANKRD11
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15569818
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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