A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638809



Internal ID7025594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:63125942..63152297hg38UCSC Ensembl
Innerchr16:63125942..63152297hg38UCSC Ensembl
Outerchr16:63125442..63152797hg38UCSC Ensembl
chr16:63159846..63186201hg19UCSC Ensembl
Innerchr16:63159846..63186201hg19UCSC Ensembl
Outerchr16:63159346..63186701hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3826356
hg1926356
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15498484
SamplesHG02890
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638809
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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