A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18074447



Internal ID20641487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:44570675..44571799hg38UCSC Ensembl
chr22:44966555..44967679hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg381125
hg191125
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6538209
Supporting Variants
Samples
Known GenesLINC00207
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18074447
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