A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4738429



Internal ID20514397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:33563392..33563443hg38UCSC Ensembl
chr21:34935698..34935749hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16293961
Samples
Known GenesSON
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4738429
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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