A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5638404



Internal ID21586709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:3509692..3509692hg38UCSC Ensembl
chr5:3509806..3509806hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17124222
SamplesHG03486
Known GenesLINC01019
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5638404
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer