A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18073947



Internal ID20640987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38171724..38177842hg38UCSC Ensembl
chr22:38567731..38573849hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg386119
hg196119
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6553537
Supporting Variants
Samples
Known GenesPLA2G6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18073947
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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