A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17843643



Internal ID22027286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:114755576..114755576hg38UCSC Ensembl
chr10:116515335..116515335hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6247551
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17843643
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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