A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17404008



Internal ID22461878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:37935368..37935659hg38UCSC Ensembl
chr22:38331375..38331666hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg38292
hg19292
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5955834
Supporting Variants
Samples
Known GenesMICALL1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17404008
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer