A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17110010



Internal ID21450882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:206841615..206843390hg38UCSC Ensembl
chr2:207706339..207708114hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg381776
hg191776
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5582032
Supporting Variants
SamplesHG01505
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17110010
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