A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5971824



Internal ID22746759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:41500397..41500397hg38UCSC Ensembl
chr11:41521947..41521947hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38190
hg19190
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17356018
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5971824
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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