A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17143213



Internal ID21453834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:107368450..107368499hg38UCSC Ensembl
chr8:108380678..108380727hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5582330
Supporting Variants
SamplesHG02011
Known GenesANGPT1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17143213
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