A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4744396



Internal ID20520395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32123868..32123933hg38UCSC Ensembl
chr1:32589469..32589534hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16283821
Samples
Known GenesKPNA6
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4744396
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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