A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5955571



Internal ID22730772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:11767626..11767626hg38UCSC Ensembl
chr3:11809100..11809100hg19UCSC Ensembl
Cytoband3p25.2
Allele length
AssemblyAllele length
hg38166
hg19166
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17398006
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5955571
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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