A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17103167



Internal ID21485171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:14243837..14244052hg38UCSC Ensembl
chr19:14354649..14354864hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38216
hg19216
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5586917
Supporting Variants
SamplesNA12329
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17103167
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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