A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17420284



Internal ID22478154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:30275824..30286902hg38UCSC Ensembl
chr3:30317315..30328393hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3811079
hg1911079
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5901505
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17420284
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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