A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4433351



Internal ID21395353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:36303685..36303985hg38UCSC Ensembl
chr21:37675983..37676283hg19UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv470n172
Supporting Variantsnssv15751144
SamplesMDQ045
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4433351
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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