A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17402430



Internal ID22460300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:27203790..27205183hg38UCSC Ensembl
chr22:27599752..27601145hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg381394
hg191394
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5950027
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17402430
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