A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5922277



Internal ID22697502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33792986..33805009hg38UCSC Ensembl
chr11:33814532..33826555hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3812024
hg1912024
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17360415
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5922277
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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