A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17987852



Internal ID20554892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:124964172..124970970hg38UCSC Ensembl
chr11:124834068..124840866hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg386799
hg196799
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6464457
Supporting Variants
Samples
Known GenesCCDC15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17987852
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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