A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5482137



Internal ID259597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:104953958..105004211hg38UCSC Ensembl
chr9:107716239..107766492hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3850254
hg1950254
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17026625
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5482137
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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