A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15484690



Internal ID5236024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57298455..57300333hg38UCSC Ensembl
Innerchr16:57298455..57300333hg38UCSC Ensembl
Outerchr16:57298235..57300556hg38UCSC Ensembl
chr16:57332367..57334245hg19UCSC Ensembl
Innerchr16:57332367..57334245hg19UCSC Ensembl
Outerchr16:57332147..57334468hg19UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg381879
hg191879
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3638710
Supporting Variants
SamplesNA18628
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15484690
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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