A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17367306



Internal ID22592975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:69073780..69073831hg38UCSC Ensembl
chr11:68841248..68841299hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5922372
Supporting Variants
Samples
Known GenesTPCN2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17367306
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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