A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17849898



Internal ID22033541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:43610545..43610545hg38UCSC Ensembl
chr19:44114697..44114697hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6251064
Supporting Variants
Samples
Known GenesZNF428
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17849898
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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