A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16897200



Internal ID172279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:222755762..222755813hg38UCSC Ensembl
chr1:222929104..222929155hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38213
hg19213
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5544760
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16897200
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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