A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18074909



Internal ID20641949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:37485201..37486600hg38UCSC Ensembl
chr22:37881239..37882638hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6552315
Supporting Variants
Samples
Known GenesMFNG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18074909
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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