A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17482433



Internal ID22540338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:89010282..89012901hg38UCSC Ensembl
chr1:89475965..89478584hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg382620
hg192620
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5830843
Supporting Variants
Samples
Known GenesGBP3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17482433
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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