A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17989514



Internal ID20556554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:22124501..22125400hg38UCSC Ensembl
chr11:22146047..22146946hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6438956
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17989514
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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