A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17107071



Internal ID21449439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:876864..876864hg38UCSC Ensembl
chr19:876864..876864hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5648720
Supporting Variants
SamplesHG01114
Known GenesMED16
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17107071
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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