A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17154842



Internal ID21480646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:37506364..37506364hg38UCSC Ensembl
chr8:37363882..37363882hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5642831
Supporting Variants
SamplesHG03683
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17154842
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer