A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17139362



Internal ID21411518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:124750175..124750269hg38UCSC Ensembl
chr3:124469022..124469116hg19UCSC Ensembl
Cytoband3q21.2
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5581291
Supporting Variants
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17139362
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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