A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17119087



Internal ID21458740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:36645818..36645818hg38UCSC Ensembl
chr21:38018116..38018116hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5664913
Supporting Variants
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17119087
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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