A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17986888



Internal ID20553928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:113843871..113846822hg38UCSC Ensembl
chr11:113714593..113717544hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg382952
hg192952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6472864
Supporting Variants
Samples
Known GenesUSP28
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17986888
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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