A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5578304



Internal ID21526769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:25634224..25634334hg38UCSC Ensembl
chr2:25857093..25857203hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17112754
SamplesNA18939
Known GenesDTNB
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5578304
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