A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638201



Internal ID6678299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:22179730..22188051hg38UCSC Ensembl
Innerchr16:22179730..22188051hg38UCSC Ensembl
Outerchr16:22179522..22188277hg38UCSC Ensembl
chr16:22191051..22199372hg19UCSC Ensembl
Innerchr16:22191051..22199372hg19UCSC Ensembl
Outerchr16:22190843..22199598hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg388322
hg198322
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15416378
SamplesNA19679
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638201
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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