A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15552550



Internal ID4910748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:86075518..86086080hg38UCSC Ensembl
Innerchr16:86075518..86086080hg38UCSC Ensembl
Outerchr16:86075018..86086580hg38UCSC Ensembl
chr16:86109124..86119686hg19UCSC Ensembl
Innerchr16:86109124..86119686hg19UCSC Ensembl
Outerchr16:86108624..86120186hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3810563
hg1910563
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3639475
Supporting Variants
SamplesNA12749
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15552550
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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