A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17135010



Internal ID21462932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:31870657..31870817hg38UCSC Ensembl
chr3:31912149..31912309hg19UCSC Ensembl
Cytoband3p23
Allele length
AssemblyAllele length
hg38161
hg19161
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5582079
Supporting Variants
SamplesHG03009
Known GenesOSBPL10
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17135010
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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