A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17842403



Internal ID22026046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91701912..91701912hg38UCSC Ensembl
chr10:93461669..93461669hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg38179
hg19179
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6247371
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17842403
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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