A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638884



Internal ID7025669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67346423..67348933hg38UCSC Ensembl
Innerchr16:67346478..67348878hg38UCSC Ensembl
Outerchr16:67346368..67348988hg38UCSC Ensembl
chr16:67380326..67382836hg19UCSC Ensembl
Innerchr16:67380381..67382781hg19UCSC Ensembl
Outerchr16:67380271..67382891hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg382511
hg192511
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15501427
SamplesHG04212
Known GenesLRRC36
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638884
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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