A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17841925



Internal ID22025568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:63149760..63149760hg38UCSC Ensembl
chr10:64909520..64909520hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38244
hg19244
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6247147
Supporting Variants
Samples
Known GenesNRBF2
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17841925
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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