A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5885905



Internal ID22660891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:140003..143030hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg383028
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv859n209
Supporting Variantsnssv17480365
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5885905
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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