A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17846619



Internal ID22030262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:51957543..51957543hg38UCSC Ensembl
chr15:52249740..52249740hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6242071
Supporting Variants
Samples
Known GenesLEO1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17846619
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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