A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17120630



Internal ID21439410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:16323394..16323513hg38UCSC Ensembl
chr4:16325017..16325136hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5569854
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17120630
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