A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17131358



Internal ID21451721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:187755899..187755899hg38UCSC Ensembl
chr3:187473687..187473687hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg38379
hg19379
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5615071
Supporting Variants
SamplesHG01596
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17131358
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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