A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5493744



Internal ID270911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96594520..96606204hg38UCSC Ensembl
chr9:99356802..99368486hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3811685
hg1911685
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17026811
Samples
Known GenesCDC14B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5493744
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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