A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17356171



Internal ID22581840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47194576..47197718hg38UCSC Ensembl
chr11:47216127..47219269hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg383143
hg193143
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5913527
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17356171
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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