A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17989905



Internal ID20556945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:36124846..36136827hg38UCSC Ensembl
chr11:36146396..36158377hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3811982
hg1911982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6472886
Supporting Variants
Samples
Known GenesLDLRAD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17989905
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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