A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5476752



Internal ID254358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:111387040..111387791hg38UCSC Ensembl
chr9:114149320..114150071hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38752
hg19752
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17026260
Samples
Known GenesKIAA0368
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5476752
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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