A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453223



Internal ID21110776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128535157..128537408hg38UCSC Ensembl
chr9:131297436..131299687hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg382252
hg192252
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18176884
Samples
Known GenesGLE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453223
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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