A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5920494



Internal ID22695717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121327716..121327850hg38UCSC Ensembl
chr9:124089994..124090128hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17436405
Samples
Known GenesGSN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5920494
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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