A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6542890



Internal ID20916141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:30411563..30412578hg38UCSC Ensembl
chr22:30807552..30808567hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg381016
hg191016
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073677
Samples
Known GenesSEC14L2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6542890
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