A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548356



Internal ID20921543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:40046791..40051121hg38UCSC Ensembl
chr22:40442795..40447125hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg384331
hg194331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073805
Samples
Known GenesTNRC6B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548356
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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