A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17130051



Internal ID21451364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:46201409..46201409hg38UCSC Ensembl
chr21:47621323..47621323hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38271
hg19271
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5665680
Supporting Variants
SamplesHG01505
Known GenesLSS
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17130051
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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