A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6550807



Internal ID20923948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:17636020..17646733hg38UCSC Ensembl
chr22:18118786..18129499hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3810714
hg1910714
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18071605
Samples
Known GenesBCL2L13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6550807
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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