A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17158971



Internal ID21509387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:66618441..66624225hg38UCSC Ensembl
chr8:67530676..67536460hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg385785
hg195785
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5568439
Supporting Variants
SamplesNA20847
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17158971
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