A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18072995



Internal ID20640035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:29056350..29061462hg38UCSC Ensembl
chr22:29452338..29457450hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg385113
hg195113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6554819
Supporting Variants
Samples
Known GenesC22orf31, ZNRF3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18072995
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