A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5957354



Internal ID22732478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:108022201..108022201hg38UCSC Ensembl
chr4:108943357..108943357hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17424366
Samples
Known GenesHADH
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5957354
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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