A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637908



Internal ID6678008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10605746..10634776hg38UCSC Ensembl
Innerchr16:10605746..10634776hg38UCSC Ensembl
Outerchr16:10605246..10635276hg38UCSC Ensembl
chr16:10699603..10728633hg19UCSC Ensembl
Innerchr16:10699603..10728633hg19UCSC Ensembl
Outerchr16:10699103..10729133hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3829031
hg1929031
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15373035
SamplesNA19779
Known GenesTEKT5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637908
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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