A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5574018



Internal ID21522429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:53699685..53701614hg38UCSC Ensembl
chr4:54565852..54567781hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg381930
hg191930
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17126105
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5574018
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