A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17059797



Internal ID21470034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:117029192..117029256hg38UCSC Ensembl
chr1:117571814..117571878hg19UCSC Ensembl
Cytoband1p13.1
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5571189
Supporting Variants
SamplesHG03125
Known GenesCD101
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17059797
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