A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17135231



Internal ID21478701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:153373294..153373294hg38UCSC Ensembl
chr3:153091083..153091083hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg38509
hg19509
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5617958
Supporting Variants
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17135231
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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