A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548846



Internal ID20922024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:41373745..41378595hg38UCSC Ensembl
chr22:41769749..41774599hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg384851
hg194851
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18074502
Samples
Known GenesTEF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548846
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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