A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17990171



Internal ID20557213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:22445338..22452614hg38UCSC Ensembl
chr11:22466884..22474160hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg387277
hg197277
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6442292
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17990171
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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