A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5926127



Internal ID22701354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:104874758..104874849hg38UCSC Ensembl
chr9:107637039..107637130hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17429694
Samples
Known GenesABCA1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5926127
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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