A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5489104



Internal ID266393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:131964352..131965735hg38UCSC Ensembl
chr9:134839739..134841122hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg381384
hg191384
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17029948
Samples
Known GenesMED27
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5489104
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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