A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17111450



Internal ID21489339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:219067056..219067339hg38UCSC Ensembl
chr2:219931778..219932061hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38284
hg19284
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5581244
Supporting Variants
SamplesNA18939
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17111450
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