A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544225



Internal ID20917464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:29447519..29451571hg38UCSC Ensembl
chr22:29843508..29847560hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg384053
hg194053
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073017
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544225
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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