A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6545765



Internal ID20918991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:17569129..17570605hg38UCSC Ensembl
chr22:18049194..18050670hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg381477
hg191477
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18071595
Samples
Known GenesSLC25A18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6545765
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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