A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17410071



Internal ID22467941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:182522206..182522810hg38UCSC Ensembl
chr3:182239994..182240598hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg38605
hg19605
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5904667
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17410071
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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