A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4738522



Internal ID20514492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28758751..28764660hg38UCSC Ensembl
chr1:29085263..29091172hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg385910
hg195910
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16289883
Samples
Known GenesYTHDF2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4738522
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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