A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17451201



Internal ID22509073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18504789..18506819hg38UCSC Ensembl
chr11:18526336..18528366hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg382031
hg192031
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5863303
Supporting Variants
Samples
Known GenesTSG101
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17451201
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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