A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5605575



Internal ID21553880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1123198..1123198hg38UCSC Ensembl
chr4:1116986..1116986hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17133892
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5605575
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