A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17481852



Internal ID22539757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:86802033..86808664hg38UCSC Ensembl
chr1:87267716..87274347hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg386632
hg196632
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5830784
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17481852
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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