A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5887317



Internal ID22662309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:83198933..83203819hg38UCSC Ensembl
chr17:81146702..81151588hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg384887
hg194887
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17476589
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5887317
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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