A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730966



Internal ID20506883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:14841947..14842100hg38UCSC Ensembl
chr21:16214268..16214421hg19UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg38154
hg19154
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16292644
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4730966
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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