A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5485215



Internal ID262611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129043837..129044063hg38UCSC Ensembl
chr9:131806116..131806342hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38227
hg19227
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17028045
Samples
Known GenesFAM73B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5485215
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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