A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880522



Internal ID22655492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:28230670..28239099hg38UCSC Ensembl
chr17:26557696..26566125hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg388430
hg198430
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17477521
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880522
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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