A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17101364



Internal ID21499651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:59779014..59779070hg38UCSC Ensembl
chr18:57446246..57446302hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5588055
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17101364
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