A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17110513



Internal ID21459791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:15611589..15611989hg38UCSC Ensembl
chr2:15751713..15752113hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg38401
hg19401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5569117
Supporting Variants
SamplesHG02818
Known GenesDDX1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17110513
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