A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5572897



Internal ID21521292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:54107925..54108027hg38UCSC Ensembl
chr4:54974092..54974194hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17137951
SamplesNA18939
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5572897
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