A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18072861



Internal ID20639901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:17969767..17972522hg38UCSC Ensembl
chr22:18452533..18455288hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg382756
hg192756
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6536452
Supporting Variants
Samples
Known GenesMICAL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18072861
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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