A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5861492



Internal ID22636427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:17441889..17447910hg38UCSC Ensembl
chr9:17441887..17447908hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg386022
hg196022
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17512032, nssv17512033
Samples
Known GenesCNTLN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5861492
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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