A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17407613



Internal ID22465483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:129171280..129171444hg38UCSC Ensembl
chr3:128890123..128890287hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg38165
hg19165
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5895789
Supporting Variants
Samples
Known GenesCNBP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17407613
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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