A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15378569



Internal ID2997754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:13674706..13675593hg38UCSC Ensembl
Innerchr16:13674714..13675586hg38UCSC Ensembl
Outerchr16:13674699..13675601hg38UCSC Ensembl
chr16:13768563..13769450hg19UCSC Ensembl
Innerchr16:13768571..13769443hg19UCSC Ensembl
Outerchr16:13768556..13769458hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg38888
hg19888
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637989
Supporting Variants
SamplesHG02646
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15378569
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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