A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17135764



Internal ID21456730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:123999901..123999901hg38UCSC Ensembl
chr3:123718748..123718748hg19UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg38916
hg19916
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5616042
Supporting Variants
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17135764
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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