A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17987036



Internal ID20554077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:121818051..121818634hg38UCSC Ensembl
chr11:121688759..121689342hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg38584
hg19584
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6458869
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17987036
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00042


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