A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5875866



Internal ID22650825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:43872192..43874491hg38UCSC Ensembl
chr17:41949560..41951859hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474366
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5875866
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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