A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6053184



Internal ID21962418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:33563396..33563447hg38UCSC Ensembl
chr21:34935702..34935753hg19UCSC 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 Variantsnssv17647150
Samples
Known GenesSON
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6053184
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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