A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4389272



Internal ID21380407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:154854807..154854999hg38UCSC Ensembl
chr1:154827283..154827475hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38193
hg19193
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15703960
Samples
Known GenesKCNN3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4389272
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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