A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17425659



Internal ID22483529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:162497119..163281467hg38UCSC Ensembl
chr3:162214907..162999255hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38784349
hg19784349
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5887660
Supporting Variants
Samples
Known GenesCT64
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17425659
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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