A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17854934



Internal ID22038577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:58568659..58568659hg38UCSC Ensembl
chr3:58554386..58554386hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg38213
hg19213
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6254069
Supporting Variants
Samples
Known GenesFAM107A
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17854934
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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