A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17065460



Internal ID21504833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:55361866..55362044hg38UCSC Ensembl
chr1:55827539..55827717hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg38179
hg19179
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5570613
Supporting Variants
SamplesNA19650
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17065460
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