A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638395



Internal ID7025181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:31238774..31250830hg38UCSC Ensembl
Innerchr16:31238824..31250780hg38UCSC Ensembl
Outerchr16:31238704..31250900hg38UCSC Ensembl
chr16:31250095..31262151hg19UCSC Ensembl
Innerchr16:31250145..31262101hg19UCSC Ensembl
Outerchr16:31250025..31262221hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3812057
hg1912057
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15441834
SamplesNA18623
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638395
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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