A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5954824



Internal ID22730052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:113954448..113954448hg38UCSC Ensembl
chr4:114875604..114875604hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17425530
Samples
Known GenesARSJ
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5954824
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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