A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17849744



Internal ID22033387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:26745629..26745629hg38UCSC Ensembl
chr18:24325593..24325593hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6259274
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17849744
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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