A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17061901



Internal ID21454282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:197180632..197180632hg38UCSC Ensembl
chr1:197149762..197149762hg19UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg382392
hg192392
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5612093
Supporting Variants
SamplesHG02011
Known GenesZBTB41
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17061901
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