A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15373034



Internal ID6056374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10584644..10592593hg38UCSC Ensembl
Innerchr16:10584644..10592593hg38UCSC Ensembl
Outerchr16:10584144..10593093hg38UCSC Ensembl
chr16:10678501..10686450hg19UCSC Ensembl
Innerchr16:10678501..10686450hg19UCSC Ensembl
Outerchr16:10678001..10686950hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg387950
hg197950
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637907
Supporting Variants
SamplesNA19451
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15373034
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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