A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17851109



Internal ID22034752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:206130041..206130041hg38UCSC Ensembl
chr2:206994765..206994765hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6253280
Supporting Variants
Samples
Known GenesNDUFS1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17851109
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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