A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18073990



Internal ID20641030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38685756..38691122hg38UCSC Ensembl
chr22:39081761..39087127hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg385367
hg195367
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6546014
Supporting Variants
Samples
Known GenesJOSD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18073990
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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