A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4751384



Internal ID20527244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:83342142..83342142hg38UCSC Ensembl
chr15:84010894..84010894hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16293226
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4751384
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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