A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17064489



Internal ID21415245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26905651..26905651hg38UCSC Ensembl
chr1:27232142..27232142hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38207
hg19207
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5606827
Supporting Variants
SamplesHG00514
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17064489
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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