A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17061498



Internal ID21439933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:163037800..163037855hg38UCSC Ensembl
chr1:163007590..163007645hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5578990
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17061498
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