A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17131288



Internal ID21474232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:30824288..30824776hg38UCSC Ensembl
chr3:30865780..30866268hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg38489
hg19489
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5571375
Supporting Variants
SamplesHG03371
Known GenesGADL1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17131288
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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