A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17082736



Internal ID21479010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:111874519..111874519hg38UCSC Ensembl
chr13:112528833..112528833hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5651083
Supporting Variants
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17082736
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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