A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5574524



Internal ID21522940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:221860801..221861132hg38UCSC Ensembl
chr1:222034143..222034474hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17063411
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5574524
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