A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5478784



Internal ID256331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121173733..121174768hg38UCSC Ensembl
chr9:123936011..123937046hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg381036
hg191036
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17028531
Samples
Known GenesCNTRL
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5478784
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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