A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5489950



Internal ID267215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97896725..97896911hg38UCSC Ensembl
chr9:100659007..100659193hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38187
hg19187
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17026857
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5489950
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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