A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17991058



Internal ID20558098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:40110501..40111200hg38UCSC Ensembl
chr11:40132051..40132750hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6471539
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17991058
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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