A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5953768



Internal ID22729043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:194498482..194498482hg38UCSC Ensembl
chr3:194219211..194219211hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38252
hg19252
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17416587
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5953768
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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