A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17418105



Internal ID22475975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:68798472..68799688hg38UCSC Ensembl
chr3:68847623..68848839hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg381217
hg191217
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5905790
Supporting Variants
Samples
Known GenesFAM19A4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17418105
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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