A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17089456



Internal ID21413072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:75910079..75910079hg38UCSC Ensembl
chr13:76484215..76484215hg19UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5664330
Supporting Variants
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17089456
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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