A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17839060



Internal ID22022703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:167889451..167889451hg38UCSC Ensembl
chr1:167858689..167858689hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg38239
hg19239
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6245573
Supporting Variants
Samples
Known GenesADCY10
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17839060
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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