A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17496844



Internal ID22554778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:91444398..91451770hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg387373
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5837453
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17496844
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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