A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17135276



Internal ID21468874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:186015086..186015086hg38UCSC Ensembl
chr3:185732875..185732875hg19UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5619071
Supporting Variants
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17135276
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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