A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637910



Internal ID7024698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10651762..10653765hg38UCSC Ensembl
Innerchr16:10651812..10653715hg38UCSC Ensembl
Outerchr16:10651710..10653817hg38UCSC Ensembl
chr16:10745619..10747622hg19UCSC Ensembl
Innerchr16:10745669..10747572hg19UCSC Ensembl
Outerchr16:10745567..10747674hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg382004
hg192004
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15373046, essv15373044, essv15373045, essv15373041, essv15373042, essv15373043
SamplesHG03999, HG03691, HG03730, HG03866, HG03689, HG03863
Known GenesTEKT5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637910
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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