A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18074364



Internal ID20641404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:42967866..42972877hg38UCSC Ensembl
chr22:43363872..43368883hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg385012
hg195012
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6538616
Supporting Variants
Samples
Known GenesPACSIN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18074364
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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