A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17106507



Internal ID21463932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:58595895..58599660hg38UCSC Ensembl
chr19:59107262..59111027hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg383766
hg193766
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5592521
Supporting Variants
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17106507
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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