A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17849571



Internal ID22033214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:5927404..5927404hg38UCSC Ensembl
chr19:5927415..5927415hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6242757
Supporting Variants
Samples
Known GenesRANBP3
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17849571
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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