A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6550294



Internal ID20923443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38793801..38794300hg38UCSC Ensembl
chr22:39189806..39190305hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073996
Samples
Known GenesDNAL4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6550294
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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