A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5926141



Internal ID22701368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:5684451..5689210hg38UCSC Ensembl
chr9:5684451..5689210hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg384760
hg194760
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17446836
Samples
Known GenesKIAA1432
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5926141
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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