A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17990151



Internal ID20557193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:2836007..2837123hg38UCSC Ensembl
chr11:2857237..2858353hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381117
hg191117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6446530
Supporting Variants
Samples
Known GenesKCNQ1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17990151
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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