A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637909



Internal ID7024697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10632967..10636172hg38UCSC Ensembl
Innerchr16:10632967..10636172hg38UCSC Ensembl
Outerchr16:10632857..10636298hg38UCSC Ensembl
chr16:10726824..10730029hg19UCSC Ensembl
Innerchr16:10726824..10730029hg19UCSC Ensembl
Outerchr16:10726714..10730155hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg383206
hg193206
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15373036, essv15373040, essv15373039, essv15373038, essv15373037
SamplesHG03559, HG03378, HG01462, HG02010, HG03279
Known GenesTEKT5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637909
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer