A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17117158



Internal ID21472837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:58648367..58648564hg38UCSC Ensembl
chr20:57223423..57223620hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg38198
hg19198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5589705
Supporting Variants
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17117158
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