A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17133729



Internal ID21472366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32537906..32538033hg38UCSC Ensembl
chr3:32579398..32579525hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5582136
Supporting Variants
SamplesHG03125
Known GenesDYNC1LI1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17133729
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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