A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5951825



Internal ID22727170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:25988555..25988555hg38UCSC Ensembl
chr4:25990177..25990177hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38256
hg19256
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17414317
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5951825
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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