A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5488544



Internal ID265852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:67633387..67641550hg38UCSC Ensembl
chr9:46291909..46300061hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg388164
hg198153
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17024217
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5488544
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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