A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5972326



Internal ID22747261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95271666..95271666hg38UCSC Ensembl
chr11:95004830..95004830hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17364882
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5972326
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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