A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4757241



Internal ID20533101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68258556..68258556hg38UCSC Ensembl
chr15:68550894..68550894hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16273326
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4757241
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