A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18028287



Internal ID20595327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10646587..10657688hg38UCSC Ensembl
chr16:10740444..10751545hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3811102
hg1911102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6514539
Supporting Variants
Samples
Known GenesTEKT5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18028287
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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