A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17991173



Internal ID20558213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47755267..47762655hg38UCSC Ensembl
chr11:47776819..47784207hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg387389
hg197389
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6469534
Supporting Variants
Samples
Known GenesFNBP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17991173
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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