A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5959398



Internal ID22734430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:151811656..151811656hg38UCSC Ensembl
chr4:152732808..152732808hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg38403
hg19403
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17414406
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5959398
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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