A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554759



Internal ID20927850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:42370570..42391425hg38UCSC Ensembl
chr21:43790679..43811534hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3820856
hg1920856
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18072474
Samples
Known GenesTMPRSS3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554759
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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