A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17408302



Internal ID22466172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:222163724..222170816hg38UCSC Ensembl
chr2:223028443..223035535hg19UCSC Ensembl
Cytoband2q36.1
Allele length
AssemblyAllele length
hg387093
hg197093
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5893662
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17408302
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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