A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17127005



Internal ID21451872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:108034122..108034122hg38UCSC Ensembl
chr3:107752969..107752969hg19UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg381571
hg191571
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5614783
Supporting Variants
SamplesHG01596
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17127005
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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