A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536962



Internal ID20910306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:41293007..41422526hg38UCSC Ensembl
chr21:42664934..42794453hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38129520
hg19129520
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18071487
Samples
Known GenesFAM3B, MX1, MX2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536962
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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