A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730402



Internal ID20506314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:21461252..21461316hg38UCSC Ensembl
chr1:21787745..21787809hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16276059
Samples
Known GenesNBPF3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4730402
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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