A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18074547



Internal ID20641587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:42015538..42016028hg38UCSC Ensembl
chr22:42411542..42412032hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg38491
hg19491
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6548817
Supporting Variants
Samples
Known GenesWBP2NL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18074547
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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