A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17992189



Internal ID20559229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:5232429..5232759hg38UCSC Ensembl
chr11:5253659..5253989hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6437559
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17992189
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00184


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