A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17062275



Internal ID21475175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:211457255..211458109hg38UCSC Ensembl
chr1:211630597..211631451hg19UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg38855
hg19855
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5574458
Supporting Variants
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17062275
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