A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17123821



Internal ID21458818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:161153458..161153458hg38UCSC Ensembl
chr3:160871246..160871246hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5623035
Supporting Variants
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17123821
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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