A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5954446



Internal ID22729690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:15903045..15903045hg38UCSC Ensembl
chr2:16043168..16043168hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg38238
hg19238
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17394057
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5954446
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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