A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553391



Internal ID20926499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:25925001..25929100hg38UCSC Ensembl
chr22:26320968..26325067hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg384100
hg194100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073146
Samples
Known GenesMYO18B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553391
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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