A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17121689



Internal ID21489358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:88419067..88430948hg38UCSC Ensembl
chr3:88468217..88480098hg19UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3811882
hg1911882
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5568946
Supporting Variants
SamplesNA18939
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17121689
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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