A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553928



Internal ID20927038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:42391680..42392124hg38UCSC Ensembl
chr21:43811789..43812233hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38445
hg19445
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18072476
Samples
Known GenesTMPRSS3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553928
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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