A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17363454



Internal ID22589123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:22699992..22699992hg38UCSC Ensembl
chr1:23026485..23026485hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5963822
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17363454
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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