A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17103048



Internal ID21471770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11302879..11304684hg38UCSC Ensembl
chr19:11413555..11415360hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381806
hg191806
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5586954
Supporting Variants
SamplesHG03125
Known GenesTSPAN16
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17103048
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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