A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5969709



Internal ID22744644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:21611994..22091393hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38479400
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17381528
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5969709
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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