A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432649



Internal ID21394651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:24323369..24324609hg38UCSC Ensembl
chr18:21903333..21904573hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg381241
hg191241
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv335n172
Supporting Variantsnssv15746874
SamplesMDQ045
Known GenesOSBPL1A
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432649
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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