A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17141025



Internal ID21419408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:63857151..63857274hg38UCSC Ensembl
chr8:64769708..64769831hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5579946
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17141025
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