A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15553965



Internal ID6296592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:86795992..86829634hg38UCSC Ensembl
Innerchr16:86796008..86829618hg38UCSC Ensembl
Outerchr16:86795976..86829650hg38UCSC Ensembl
chr16:86829598..86863240hg19UCSC Ensembl
Innerchr16:86829614..86863224hg19UCSC Ensembl
Outerchr16:86829582..86863256hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3833643
hg1933643
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3639491
Supporting Variants
SamplesNA19900
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15553965
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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