A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5571842



Internal ID21520225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:78581629..78581938hg38UCSC Ensembl
chr3:78630779..78631088hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17123380
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5571842
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