A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5951168



Internal ID22726542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:25135247..25135247hg38UCSC Ensembl
chr4:25136869..25136869hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38241
hg19241
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17426281
Samples
Known GenesSEPSECS
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5951168
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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