A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17089397



Internal ID21433118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:77430380..77430380hg38UCSC Ensembl
chr13:78004515..78004515hg19UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5659739
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17089397
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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