A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5479532



Internal ID257051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:137406254..137407009hg38UCSC Ensembl
chr9:140300706..140301461hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38756
hg19756
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17029694
Samples
Known GenesEXD3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5479532
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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