A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17139261



Internal ID21450378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:146032178..146032178hg38UCSC Ensembl
chr3:145749965..145749965hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38406
hg19406
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5612007
Supporting Variants
SamplesHG01114
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17139261
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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