A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17496756



Internal ID22554690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:89482223..89492321hg38UCSC Ensembl
chr3:89531373..89541471hg19UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3810099
hg1910099
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5837156
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17496756
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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