A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17986889



Internal ID20553929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:113875001..113875900hg38UCSC Ensembl
chr11:113745723..113746622hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6466201
Supporting Variants
Samples
Known GenesUSP28
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17986889
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.08154


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