A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638920



Internal ID7025705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69054207..69059348hg38UCSC Ensembl
Innerchr16:69054707..69058848hg38UCSC Ensembl
Outerchr16:69053207..69060348hg38UCSC Ensembl
chr16:69088110..69093251hg19UCSC Ensembl
Innerchr16:69088610..69092751hg19UCSC Ensembl
Outerchr16:69087110..69094251hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg385142
hg195142
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15501992
SamplesHG02757
Known GenesTANGO6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638920
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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