A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16901173



Internal ID1594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24140987..24140987hg38UCSC Ensembl
chr1:24467477..24467477hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38719
hg19719
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5549060
Supporting Variants
Samples
Known GenesIL22RA1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16901173
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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