A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17103373



Internal ID21471829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:17167071..17167071hg38UCSC Ensembl
chr19:17277881..17277881hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5655971
Supporting Variants
SamplesHG03125
Known GenesMYO9B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17103373
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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