A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17090491



Internal ID21432615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:37215555..37215555hg38UCSC Ensembl
chr13:37789692..37789692hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38168
hg19168
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5662303
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17090491
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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