A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638222



Internal ID6678320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:22821373..22839725hg38UCSC Ensembl
Innerchr16:22821378..22839721hg38UCSC Ensembl
Outerchr16:22821369..22839730hg38UCSC Ensembl
chr16:22832694..22851046hg19UCSC Ensembl
Innerchr16:22832699..22851042hg19UCSC Ensembl
Outerchr16:22832690..22851051hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg3818353
hg1918353
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15424004
SamplesHG01861
Known GenesHS3ST2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638222
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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