A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5963303



Internal ID22738238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:4612604..4612604hg38UCSC Ensembl
chr2:4660194..4660194hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17396111
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5963303
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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