A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5951155



Internal ID22726529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32397296..32397296hg38UCSC Ensembl
chr3:32438788..32438788hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38282
hg19282
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17420714
Samples
Known GenesCMTM7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5951155
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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