A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17842375



Internal ID22026018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:41059225..41059225hg38UCSC Ensembl
chr11:41080775..41080775hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38276
hg19276
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6248016
Supporting Variants
Samples
Known GenesLRRC4C
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17842375
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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