A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17993452



Internal ID20560492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63036839..63065856hg38UCSC Ensembl
chr11:62804311..62833328hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3829018
hg1929018
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6463221
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17993452
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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