A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17105744



Internal ID21508123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:540185..540789hg38UCSC Ensembl
chr19:540185..540789hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38605
hg19605
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5593926
Supporting Variants
SamplesNA20509
Known GenesCDC34
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17105744
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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