A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17138910



Internal ID21462345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:104265599..104265599hg38UCSC Ensembl
chr3:103984443..103984443hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5621123
Supporting Variants
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17138910
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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