A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5963871



Internal ID22738807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:41475509..41475638hg38UCSC Ensembl
chr21:42847436..42847565hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17405040
Samples
Known GenesTMPRSS2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5963871
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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