A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548168



Internal ID20921364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:41185740..41210105hg38UCSC Ensembl
chr22:41581744..41606109hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3824366
hg1924366
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18074488
Samples
Known GenesL3MBTL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548168
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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