A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17989061



Internal ID20556101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:24636823..24642803hg38UCSC Ensembl
chr11:24658369..24664349hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg385981
hg195981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6448325
Supporting Variants
Samples
Known GenesLUZP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17989061
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00673


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