A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17116021



Internal ID21452675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:97768779..97768972hg38UCSC Ensembl
chr2:98385242..98385435hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg38194
hg19194
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5584196
Supporting Variants
SamplesHG01596
Known GenesTMEM131
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17116021
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