A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17120687



Internal ID21482715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:70871596..70871720hg38UCSC Ensembl
chr3:70920747..70920871hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5575559
Supporting Variants
SamplesHG03732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17120687
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