A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5954352



Internal ID22729597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:165255668..165255668hg38UCSC Ensembl
chr5:164682674..164682674hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38244
hg19244
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17413545
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5954352
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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