A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17360998



Internal ID22586667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:36484987..36487125hg38UCSC Ensembl
chr11:36506537..36508675hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg382139
hg192139
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5911437
Supporting Variants
Samples
Known GenesTRAF6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17360998
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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