A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4737101



Internal ID20513058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:17911077..17911190hg38UCSC Ensembl
chr21:19283394..19283507hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16275160
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4737101
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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