A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637912



Internal ID7024700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10691857..10702188hg38UCSC Ensembl
Innerchr16:10691907..10702138hg38UCSC Ensembl
Outerchr16:10691807..10702238hg38UCSC Ensembl
chr16:10785714..10796045hg19UCSC Ensembl
Innerchr16:10785764..10795995hg19UCSC Ensembl
Outerchr16:10785664..10796095hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3810332
hg1910332
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15374021
SamplesHG01878
Known GenesTEKT5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637912
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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