A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17854035



Internal ID22037678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:218890253..218890253hg38UCSC Ensembl
chr2:219754975..219754975hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38140
hg19140
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6253403
Supporting Variants
Samples
Known GenesWNT10A
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17854035
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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