A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17849625



Internal ID22033268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16073179..16073179hg38UCSC Ensembl
chr19:16183989..16183989hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38268
hg19268
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6242815
Supporting Variants
Samples
Known GenesTPM4
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17849625
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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