A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17082254



Internal ID21441382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109010957..109010957hg38UCSC Ensembl
chr13:109663305..109663305hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5653480
Supporting Variants
SamplesHG00732
Known GenesMYO16
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17082254
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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