A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17427202



Internal ID22485072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:169485667..169486040hg38UCSC Ensembl
chr3:169203455..169203828hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg38374
hg19374
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5902122
Supporting Variants
Samples
Known GenesMECOM
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17427202
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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