A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5581716



Internal ID21530220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:576901..576950hg38UCSC Ensembl
chr4:570690..570739hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17131541
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5581716
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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