A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17990133



Internal ID20557175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:28251943..28261427hg38UCSC Ensembl
chr11:28273490..28282974hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg389485
hg199485
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6451798
Supporting Variants
Samples
Known GenesMETTL15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17990133
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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