A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17841974



Internal ID22025617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:99584424..99584424hg38UCSC Ensembl
chr10:101344181..101344181hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38165
hg19165
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6247425
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17841974
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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