A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6049870



Internal ID21959103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:39357624..39357688hg38UCSC Ensembl
chr22:39753629..39753693hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17637815
Samples
Known GenesSYNGR1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6049870
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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