A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17127408



Internal ID21469079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:182721174..182721174hg38UCSC Ensembl
chr3:182438962..182438962hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5619114
Supporting Variants
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17127408
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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