A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15379367



Internal ID5006114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14405864..14411282hg38UCSC Ensembl
Innerchr16:14405901..14411246hg38UCSC Ensembl
Outerchr16:14405828..14411319hg38UCSC Ensembl
chr16:14499721..14505139hg19UCSC Ensembl
Innerchr16:14499758..14505103hg19UCSC Ensembl
Outerchr16:14499685..14505176hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg385419
hg195419
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3638007
Supporting Variants
SamplesNA18505
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15379367
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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