A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5959369



Internal ID22734401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:43701500..43717832hg38UCSC Ensembl
chr21:45121381..45137713hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3816333
hg1916333
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17390975
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5959369
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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