A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17359213



Internal ID22584882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47252391..47253087hg38UCSC Ensembl
chr11:47273942..47274638hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38697
hg19697
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5921736
Supporting Variants
Samples
Known GenesNR1H3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17359213
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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