A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17849632



Internal ID22033275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:17166399..17166399hg38UCSC Ensembl
chr19:17277209..17277209hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6242822
Supporting Variants
Samples
Known GenesMYO9B
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17849632
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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