A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638710



Internal ID7025495
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15484690
SamplesNA18628
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638710
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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