A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17849872



Internal ID22033515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:39113768..39113768hg38UCSC Ensembl
chr19:39604408..39604408hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38278
hg19278
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6251039
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17849872
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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