A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17089461



Internal ID21440602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109654975..109654975hg38UCSC Ensembl
chr13:110307322..110307322hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38182
hg19182
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5645513
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17089461
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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