A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5492346



Internal ID269561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:28373205..28412491hg38UCSC Ensembl
chr9:28373203..28412489hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3839287
hg1939287
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17020287
Samples
Known GenesLINGO2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5492346
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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