A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17989224



Internal ID20556264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:20906565..20917329hg38UCSC Ensembl
chr11:20928111..20938875hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3810765
hg1910765
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6445954
Supporting Variants
Samples
Known GenesNELL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17989224
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00018


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