A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17066403



Internal ID21502741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:67228041..67228109hg38UCSC Ensembl
chr1:67693724..67693792hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5582363
Supporting Variants
SamplesNA19239
Known GenesIL23R
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17066403
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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