A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553849



Internal ID20926961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:49815361..49817754hg38UCSC Ensembl
chr22:50209009..50211402hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg382394
hg192394
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18074797
Samples
Known GenesBRD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553849
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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