A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17370366



Internal ID22596035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:90755718..90755718hg38UCSC Ensembl
chr13:91407972..91407972hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg38202
hg19202
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5980099
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17370366
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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