A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5475263



Internal ID252906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:1388362..1530232hg38UCSC Ensembl
chr9:1388362..1530232hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38141871
hg19141871
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17017794
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5475263
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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