A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17121282



Internal ID21482115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:123981979..123990770hg38UCSC Ensembl
chr3:123700826..123709617hg19UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg388792
hg198792
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5582469
Supporting Variants
SamplesHG03732
Known GenesROPN1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17121282
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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