A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17135473



Internal ID21480127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:11697..11773hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3877
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5570588
Supporting Variants
SamplesHG03683
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17135473
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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