A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16891831



Internal ID168749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:168577076..168577127hg38UCSC Ensembl
chr1:168546314..168546365hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5411855
Supporting Variants
Samples
Known GenesXCL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16891831
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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