A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17086517



Internal ID21486876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:90570764..90570764hg38UCSC Ensembl
chr13:91223018..91223018hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg38215
hg19215
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5654464
Supporting Variants
SamplesNA12878
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17086517
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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