A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18074391



Internal ID20641431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:43454060..43459126hg38UCSC Ensembl
chr22:43849960..43855026hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg385067
hg195067
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6552127
Supporting Variants
Samples
Known GenesMPPED1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18074391
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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