A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5886884



Internal ID22661873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:21461252..21461315hg38UCSC Ensembl
chr1:21787745..21787808hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17354165
Samples
Known GenesNBPF3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5886884
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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